11 Empregos para Grupo Lusíadas Saúde - Portugal

**Responsibilities**
+ Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations.
+ Provide medical oversight and review of safety documentation, including narratives, aggregate reports, annual and periodic safety reports, risk management plans, regulatory submissions, labeling, protocols, investigator brochures, and case report forms.
+ Support safety governance activities, including Data Safety Monitoring Boards, Safety Monitoring Committees, medical information escalations, pharmacovigilance oversight, and 24-hour medical support as required.
+ Serve as Global Safety Physician, project lead, or medical safety advisor, ensuring quality, compliance, operational delivery, training, stakeholder communication, and timely completion of deliverables.
+ Present safety findings and provide expert medical consultation to clients, internal teams, and cross-functional stakeholders.
+ Lead and develop medical safety teams through people management, workload planning, performance management, mentoring, training, resource allocation, and succession planning.
+ Oversee financial, operational, and quality performance of assigned projects, ensuring appropriate resourcing and regulatory compliance.
+ Contribute to business development activities, including proposals, budgeting, bid defenses, client presentations, strategic planning, and service-line growth initiatives.
+ Represent the Medical Safety function internally and externally, maintaining key stakeholder relationships and supporting organizational objectives.
+ Drive continuous improvement through awareness of industry, regulatory, and pharmacovigilance developments, and undertake special projects as required.
+ Provide global medical safety and pharmacovigilance oversight across clinical development and post-marketing programs.
+ Lead medical review of safety data, regulatory reports, risk management strategies, and benefit-risk assessments.
+ Manage medical safety projects, ensuring quality, compliance, stakeholder engagement, and on-time delivery.
+ Lead, develop, and resource teams of physicians and medical safety professionals globally.
+ Support business growth through client engagement, proposals, strategic initiatives, and service-line leadership.
**Required Knowledge, Skills & Experience**
+ Strong knowledge of global pharmacovigilance, clinical research, safety reporting, Good Clinical Practice (GCP), and applicable regulatory requirements.
+ In-depth understanding of clinical development, pharmaceutical research, and medical safety/monitoring activities.
+ Proven ability to manage multiple priorities, meet deadlines, and deliver high-quality outcomes in a complex environment.
+ Strong consulting, communication, stakeholder management, and relationship-building skills, with the ability to influence clients and cross-functional teams.
+ Demonstrated leadership capability, including people management, project oversight, financial accountability, and strategic decision-making.
+ Medical degree (MD or equivalent) from an accredited institution, with substantial clinical practice experience and/or pharmaceutical physician experience.
+ Significant experience in medical safety, pharmacovigilance, or medical monitoring within the pharmaceutical, biotechnology, CRO, or healthcare industry.
+ Current medical licensure (or equivalent professional registration) in the country of practice.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Description of Roles and Responsibilities:**
This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the SCOM or CRD, the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.
**Responsibilities include but are not limited to:**
- Ownership of country and site budgets. Development, negotiation, and completion of Clinical Trial Research Agreements (CTRA).
- Oversees and tracks clinical research-related payments. Payment reconciliation at study close-out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Financial forecasting in conjunction with SCOM /CRDs, other roles.
- Executes and oversees clinical trial country submissions and approvals for assigned protocols.
- Develops local language materials including local language Informed Consents and translations. Interacts with IRB/IEC and Regulatory Authority for assigned protocols.
- Manages country deliverables, timelines, and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.
- Contributes to the development of local SOPs. Oversees CTCs as applicable.
- Coordinates and liaises with CRM, CTC, CRA, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
- Collaborates closely with Headquarter to align country timelines for assigned protocols.
- Provides support and oversight to local vendors as applicable.
- Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management. Enters and updates country information in clinical and finance systems.
- Ownership of local regulatory and financial compliance. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.
- Required to in/directly influence investigators, external partners and country operations to adheres to budget targets and agreed payment timelines.
- Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval related interactions. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.
- Contribute or lead initiatives and projects adding value to the business
- Contributes strongly to COM team and other Country Operations roles knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement, and providing training as appropriate/required.
- Contributes to COM team knowledge by acting as buddy/mentor and sharing best practices as appropriate/required
**Experience Required:**
- 5-7 years of experience in clinical research.
- Portuguese fluent.
- Office visits required for Face-to-Face meetings.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Make this the place where** **_you_** **grow.**
Como líderes globais em inovação de negócio e tecnologia, trabalhamos com organizações de topo em todo o mundo para entregar soluções com impacto real.
Com +190.000 profissionais distribuídos por +70 países, combinamos o nosso conhecimento especializado com uma cultura que valoriza a aprendizagem, a curiosidade e a colaboração.
Lideramos a transformação e entregamos soluções seguras, inovadoras e específicas por indústria, que permitem aos negócios avançar. As nossas pessoas impulsionam tudo o que alcançamos; pensam de forma ousada para garantir resultados, assegurando que todas as vozes são ouvidas.
Estamos à procura de profissionais motivados para integrar a nossa equipa como Consultores de Negócio, atuando como especialistas em setor público e/ou saúde e colaborando com equipas multidisciplinares no desenvolvimento de soluções de negócio e tecnológicas que respondam às necessidades dos nossos clientes. Poderás fazer parte de uma equipa dedicada a transformar a sociedade através da inovação!
**A Tua Função**
-Identificar e compreender as necessidades dos clientes de setor público e saúde, concebendo e desenhando novos processos de negócio alinhados com as suas necessidades.
-Projetar e recomendar soluções que melhorem a eficiência e a eficácia dos processos de negócio, alinhando as operações às melhores práticas e aos objetivos organizacionais.
-Apoiar a implementação de iniciativas de transformação digital, ajudando os clientes setor público e saúde a adotar novas tecnologias e otimizar os sistemas existentes.
-Desenvolver e implementar estratégias para preparar e orientar os clientes em processos de mudança, assegurando a adaptação dos stakeholders aos novos processos e tecnologias.
-Acompanhar e medir o impacto das soluções implementadas, usando métricas de desempenho.
-Elaborar documentação detalhada, incluindo casos de uso, fluxos de trabalho, interfaces de utilizador e modelos de dados.
-Garantir que as soluções desenvolvidas estão em conformidade com a legislação do setor público e saúde.
-Apoiar equipas multidisciplinares, garantindo a execução eficaz dos projetos e promovendo uma cultura de colaboração e inovação.
Esta função descreve o teu ponto de partida na NTT DATA. Acreditamos em relações de longo prazo e apoiamos o teu crescimento. À medida que as tuas competências e ambições evoluem, trabalharemos contigo para identificar futuras oportunidades, projetos e trajetórias de carreira dentro da nossa organização.
**O Teu Perfil**
-Formação superior em Engenharia, Economia, Gestão, Administração Pública ou áreas afins.
-Experiência mínima de 3 anos no setor público e/ou saúde.
-Experiência comprovada em levantamento e análise de requisitos funcionais.
-Competência na criação de casos de uso, definição de regras de negócio, desenvolvimento de interfaces de utilizador e modelação de dados.
-Fortes competências de síntese analítica, planeamento e organização.
-Excelentes competências de comunicação e capacidade para trabalhar de forma colaborativa em equipas multidisciplinares.
**Valorizamos:**
-Conhecimentos de inglês (nível intermédio ou superior).
-Experiência em projetos de consultoria para clientes de setor público e/ou saúde.
-Experiência em projetos com os principais sistemas de informação utilizados em clientes de sector público e saúde.
-Formação ou certificação em metodologias de gestão de projetos, análise de negócio, agile, gestão da mudança, design thinking, desenho de processo e análise de dados.
-Familiaridade com ferramentas e metodologias de transformação de digital aplicadas ao setor público e saúde.
**Porquê escolher a NTT DATA?**
**Uma cultura colaborativa e de suporte**
Fomentamos um ambiente onde a curiosidade, a inovação, o envolvimento e o trabalho em equipa são celebrados. A nossa filosofia people-first é uma das razões pelas quais continuamos a ser reconhecidos globalmente.
**Desenvolvimento de carreira & aprendizagem contínua**
Acede a um percurso de formação estruturado, recursos de aprendizagem contínua, avaliações anuais de desempenho e um programa de mentoria dedicado - tudo pensado para te ajudar a crescer profissionalmente e a enfrentar novos desafios.
**Equilíbrio entre vida pessoal e profissional**
Como empresa, adotamos a abordagem BeFlex, que oferece às nossas pessoas a flexibilidade de que precisam para gerir o seu dia de trabalho de forma adaptada às suas necessidades.
**Top Employer Global**
Somos orgulhosamente certificados como Global Top Employer, um reconhecimento do nosso compromisso em ser um lugar onde as pessoas podem crescer e prosperar.
**Saúde e bem-estar em primeiro lugar**
O teu bem‑estar é importante. Os colaboradores têm acesso a psicólogos certificados e workshops online sobre e para saúde mental.
**Diversidade, Equidade & Inclusão**
Comprometemo-nos a criar um local de trabalho onde todos possam prosperar, independentemente de genero, nacionalidade, orientação sexual, deficiência, idade ou trajetória de vida. A inclusão faz parte de quem somos e da forma como trabalhamos.
\#WeAreAllUnique #YouMakeUsUnique
**Identificas-te com este desafio? Candidata-te agora ou partilha com um amigo.**

**Make this the place where** **_you_** **grow.**
Como líderes globais em inovação de negócio e tecnologia, trabalhamos com organizações de topo em todo o mundo para entregar soluções com impacto real.
Com +190.000 profissionais distribuídos por +70 países, combinamos o nosso conhecimento especializado com uma cultura que valoriza a aprendizagem, a curiosidade e a colaboração.
Lideramos a transformação e entregamos soluções seguras, inovadoras e específicas por indústria, que permitem aos negócios avançar. As nossas pessoas impulsionam tudo o que alcançamos; pensam de forma ousada para garantir resultados, assegurando que todas as vozes são ouvidas.
Estamos à procura de profissionais motivados para integrar a nossa equipa como **Consultores Tecnológicos, especializados no setor público e/ou saúde.** Este papel envolve o desenvolvimento e implementação de soluções tecnológicas, colaborando com equipas multidisciplinares para responder às necessidades específicas dos nossos clientes. Poderás fazer parte de uma equipa dedicada a transformar a sociedade através da inovação!
**A Tua Função**
**-Desenvolvimento de Soluções Tecnológicas** : Conceber e implementar soluções digitais utilizando linguagens e plataformas como Java, .NET, OutSystems e tecnologias front-end para responder às necessidades dos clientes no setor público e saúde.
**-Integração de Sistemas** : Assegurar a interoperabilidade entre diferentes sistemas e plataformas, promovendo um fluxo contínuo e seguro de informação entre entidades públicas.
**-Transformação Digital** : Apoiar iniciativas de transformação digital, incluindo migração para a cloud e digitalização de processos, melhorando a eficiência e acessibilidade dos serviços públicos.
**-Automação de Processos** : Implementar soluções de automação (RPA) para otimizar processos repetitivos, reduzindo custos e aumentando a produtividade.
**-Cibersegurança** : Colaborar na implementação de medidas de cibersegurança, garantindo a proteção de sistemas e dados sensíveis no setor público e saúde.
**-Manutenção e Suporte de Sistemas** : Assegurar a continuidade dos sistemas de informação críticos, realizando manutenção preventiva e prestando suporte técnico.
Esta função descreve o teu ponto de partida na NTT DATA. Acreditamos em relações de longo prazo e apoiamos o teu crescimento. À medida que as tuas competências e ambições evoluem, trabalharemos contigo para identificar futuras oportunidades, projetos e trajetórias de carreira dentro da nossa organização.
**O Teu Perfil**
+ Formação superior em Engenharia, Informática, Matemática, Gestão ou áreas afins.
+ Conhecimentos práticos em uma ou mais das seguintes tecnologias: Java, .NET, OutSystems ou tecnologias front-end (HTML, CSS, JavaScript).
+ Conhecimento de SQL e experiência na utilização de bases de dados (PostGres, MySQL, SQL Server, Oracle).
+ Experiência de mais de 2 anos em desenvolvimento de software ou implementação de soluções tecnológicas.
+ Experiência no desenho de aplicações, incluindo a documentação dos requisitos técnicos.
+ Experiência no desenho, realização de testes e implementação de metodologias que garantam a qualidade das soluções desenvolvidas.
**Valorizamos:**
+ Experiência em projetos de consultoria tecnológica para clientes do setor público e/ou saúde.
+ Experiência nos principais sistemas de informação utilizados em clientes do setor público e saúde.
+ Experiência na realização de revisão de código.
+ Experiência na utilização de ferramentas DevOps (GIT, Jira, Confluence, Bamboo, Maven, JUnit, , Docker ou Kubernetes).
+ Experiência na utilização de infraestrutura cloud (Azure, Cloud Native, AWS, Google Cloud).
+ Conhecimentos em cibersegurança e integração de sistemas.
+ Certificações em tecnologias relevantes (Java, .NET, OutSystems) e/ou metodologias de desenvolvimento ágil.
+ Conhecimentos de inglês (nível intermédio ou superior).
**Porquê escolher a NTT DATA?**
**Uma cultura colaborativa e de suporte**
Fomentamos um ambiente onde a curiosidade, a inovação, o envolvimento e o trabalho em equipa são celebrados. A nossa filosofia people-first é uma das razões pelas quais continuamos a ser reconhecidos globalmente.
**Desenvolvimento de carreira & aprendizagem contínua**
Acede a um percurso de formação estruturado, recursos de aprendizagem contínua, avaliações anuais de desempenho e um programa de mentoria dedicado - tudo pensado para te ajudar a crescer profissionalmente e a enfrentar novos desafios.
**Equilíbrio entre vida pessoal e profissional**
Como empresa, adotamos a abordagem BeFlex, que oferece às nossas pessoas a flexibilidade de que precisam para gerir o seu dia de trabalho de forma adaptada às suas necessidades.
**Top Employer Global**
Somos orgulhosamente certificados como Global Top Employer, um reconhecimento do nosso compromisso em ser um lugar onde as pessoas podem crescer e prosperar.
**Saúde e bem-estar em primeiro lugar**
O teu bem‑estar é importante. Os colaboradores têm acesso a psicólogos certificados e workshops online sobre e para saúde mental.
**Diversidade, Equidade & Inclusão**
Comprometemo-nos a criar um local de trabalho onde todos possam prosperar, independentemente de genero, nacionalidade, orientação sexual, deficiência, idade ou trajetória de vida. A inclusão faz parte de quem somos e da forma como trabalhamos.
\#WeAreAllUnique #YouMakeUsUnique
**Identificas-te com este desafio? Candidata-te agora ou partilha com um amigo.**

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
**A Day in the Life**
At Medtronic, we strive without reserve for the greatest possible reliability and quality in our products and processes. To help ensure our patients safety and health, we closely monitor and report on our products' performance. The Patient & Technical Services department in Heerlen is responsible for addressing clinical/technical product inquiries for Europe, Middle East and Africa.
The Patient Service Representative is the central contact point for patients that have product technical and application related questions. Furthermore, the Patient Services Representative can assist healthcare professionals and Medtronic representatives with their technical questions. For this position, we expect you to be a medical technical professional with a passion for helping our Neuromodulation and Pelvic Health patients, who have an implanted neurostimulator or drug pump. Our team also supports internal and external customers with troubleshooting and technical questions on device functionality. In this position you will be trained to have an in depth understanding of product features, electromagnetic interference (EMI), alerts, and much more. You should be customer focused and have excellent communication skills to explain complicated technical issues to patients, health care professionals, and Medtronic representatives. Furthermore, you should use your communication skills to collaborate effectively with various teams to improve and expand our services and processes. We invite both experienced professionals and recent graduates to apply for this temporary position.
**Responsibilities may include the following and other duties may be assigned:**
+ Provide world class technical support to our patients and customers
+ Serve as a liaison between patients and our technical and marketing partners
+ Have in-depth knowledge of all relevant products
+ Perform technical activities requiring considerable judgement and have ownership of projects
+ Responsible for ensuring all documentation/system entries are fully complete
+ Connect easily with the stakeholders and is customer focused
**Required Knowledge and Experience:**
+ Excellent communication skills via phone and e-mail in English and a combination of Italian/Spanish, Italian/French or Spanish/French
+ Strong analytical and problem-solving skills that are balanced with speed and effectiveness
+ Highly organized with the ability to be flexible, multi-task and prioritize multiple assignments and to be able to contribute to/lead projects supporting the expansion of services in the future
+ Strong attention to detail and accuracy and a respected team player with strong interpersonal skills, who's able to establish relationships with colleagues in other countries and departments
Experience with working in a medical technical environment, in a technical support contact center and experience with analysing technical issues and processes for continuous improvement are considered advantages for this role. Besides this, proficiency in Microsoft Office and experience with Service Now are a plus.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

**Recruitment Fraud Alert**
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at .

**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Netherlands: 39,200.00 EUR - 58,800.00 EUR | Portugal: 21,600.00 EUR - 32,400.00 EUR | Spain: 27,840.00 EUR - 41,760.00 EUR |
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Manages, coordinates and evaluates medical projects for one or more programs in collaboration with management and other stakeholders to ensure consistency, alignment, and compliance of internal processes as well as optimal performance and issue resolution throughout project lifecycle. Represents the company in the medical research community and develops collaborative relationships with client company personnel.
**Essential Functions:**
+ Works independently to perform first pass review of safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. Reviews data for safety trends, coding consistencies, and potential follow up with investigator sites. Proactively identifies any potential issues and resolves or escalates as appropriate.
+ Reviews safety data and provides summations for safety review meetings.
+ Reviews designated sections of aggregate reports.
+ Independently functions as the Project Lead for medical monitoring services when SAE case processing has not been contracted. Manages project implementation, coordination, maintenance and close out of assigned studies as applicable. Serves as the primary point of contact for clinical project teams on studies and can act as the alliance level lead on larger alliance/multi-protocol studies.
+ Creates and maintains medical management plan(s) on studies (as applicable) and ensures that the processes included in the plan document are reflective of the contract and services requested for studies that have department involvement and those that are standalone studies (ex. MM and/or MPC).
+ Works independently to monitor the project financial status, unit forecasting, actual realization, and team allocations in systems. Coordinates staff projections based on contract values and actual hours used. Escalates any financial and/or operational risks and can attend risk management meetings to discuss.
+ Independently determines hours required for out of scope work for the teams and provides this to the finance/study team for contract modifications. Attends meetings to discuss/justify the modification requirements.
+ Resolves complex problems through in-depth evaluation of various factors and offers solutions. May assist management in training and mentoring.
+ Presents at business development, client, and investigator meetings and participates in strategy/business development calls. Represents studies at risk management meetings.
**Qualifications:**
**Education and Experience:**
+ Bachelors degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years), to include 5+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills and Abilities:**
+ Advanced knowledge of GCPs for medical oversight of clinical trials
+ Knowledge of drug development and safety reporting
+ Advanced knowledge of safety data trending to include coding
+ Working knowledge of biostatistics, data management and clinical procedures
+ Excellent problem solving and critical thinking skills
+ Excellent project management and budget skills
+ Effective mentoring skills and ability to train and lead others
+ Strong oral and written communication skills
+ Strong attention to detail
+ Ability to work in a collaborative team environment
+ Ability to maintain a positive and professional demeanor in challenging circumstances
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com ( .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
MedTech Sales
**Job Sub** **Function:**
Clinical Sales - Hospital/Hospital Systems (Commission)
**Job Category:**
Professional
**All Job Posting Locations:**
Lisbon, Portugal
**Job Description:**
About the Role
We are seeking a highly motivated **Clinical Support Specialist** to join our team in Lisbon and play a critical role in supporting healthcare professionals across orthopedic and trauma procedures. This position serves as a trusted clinical partner to surgeons, operating room teams, and commercial colleagues, helping ensure the safe and effective use of innovative medical technologies that improve patient outcomes.
The ideal candidate brings strong clinical expertise, thrives in fast-paced surgical environments, and is passionate about delivering exceptional support that drives both clinical excellence and business success.
**Key Responsibilities**
Clinical Support
+ Provide expert clinical and technical support during orthopedic, trauma, spine, and related surgical procedures.
+ Ensure the proper preparation, handling, and utilization of implants, instruments, and surgical technologies.
+ Support healthcare teams in the adoption and implementation of new products, procedures, and surgical techniques.
+ Deliver in-service education and clinical training to surgeons, nurses, and operating room personnel.
+ Identify opportunities to optimize clinical workflows and share best practices to enhance outcomes and efficiency.
+ Act as a trusted resource for clinical questions and intraoperative support.
Commercial Partnership
+ Collaborate closely with Sales and Marketing teams to support business objectives and customer engagement.
+ Participate in product demonstrations, evaluations, and clinical trials.
+ Support product launches and strategic growth initiatives.
+ Gather customer feedback and provide clinical insights to support market development and innovation.
Quality, Compliance & Patient Safety
+ Ensure compliance with company policies, Healthcare Compliance requirements, and applicable regulations.
+ Maintain accurate documentation of clinical support and training activities.
+ Promote a culture of patient safety, quality, and ethical business practices.
+ Adhere to all regulatory and quality standards related to medical devices.
**Qualifications & Experience**
Required
+ Proven experience supporting surgical procedures in an operating room environment.
+ Strong understanding of surgical workflows, sterile techniques, and operating room protocols.
+ Excellent communication and interpersonal skills, with the ability to build strong relationships with healthcare professionals and cross-functional teams.
+ Demonstrated ability to quickly learn and adapt to new technologies, products, and surgical techniques.
+ Strong problem-solving skills and the ability to perform effectively under pressure in clinical settings.
+ Proactive, patient-focused mindset with a commitment to continuous learning and clinical excellence.
Preferred
+ Additional education, certification, or specialized training in Orthopedics, Trauma, Spine, Neurosurgery, or related clinical disciplines.
+ Participation in AO Spine, AO Trauma, or other internationally recognized clinical training programs.
+ Experience providing intraoperative support for implants and surgical instrumentation.
+ Previous experience within the medical device industry.
**What You'll Bring**
+ Clinical credibility and confidence in the operating room.
+ Passion for improving patient outcomes through innovative healthcare solutions.
+ Ability to work independently while collaborating effectively with diverse stakeholders.
+ A growth mindset and commitment to ongoing professional development.
+ Strong customer focus and dedication to delivering exceptional service.
On October 14, 2025, Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.
It is anticipated following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by Orthopedics employment processes, programs, policies, and benefit plans. Details of any planned changes would be provided to you by Orthopedics at an appropriate time and subject to any necessary consultation processes."
**Required Skills:**
**Preferred Skills:**
**The anticipated base pay range for this position is:**
22,200.00 - 35,535.00
**Benefits:**
In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees' and companies' performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location's eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers. ( is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com ( .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
Product Safety
**Job Sub** **Function:**
Product Safety Risk Management MD
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Lisbon, Portugal
**Job Description:**
**Medical Review Safety Physician, Manager:**
The employee is acquainted with the annual company and division goals and is aware of how he/she/they can influence these through his/her/their performance.
**Essential Job Duties and Responsibilities**
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall Pharmacovigilance process; this includes single case signal detection activities for selected products as well as operational aspects of individual case medical review.
The Medical Review Safety Physician (MRSP) manager has responsibility for determining the medical and scientific relevance of adverse event reports within the context of the product's safety profile as well as other products within the same therapeutic area. These responsibilities include spontaneous reports, clinical and non-clinical studies, literature reports and other sources of safety data. Additionally, MRSPs participate in matrix management activities (e.g. Safety Management Team (SMT) and provide pharmacovigilance expertise on individual case reports. MRSPs support activities such as evaluating safety issues from various sources including Designated Medical Events (DME) and Events of Interest (EVOI), preparation of aggregate safety reports such as PBRERs/PADERs, ad-hoc regulatory reports, Risk Management Plans, and interpretation of surveillance and product quality data.
· Active participation in MRSP activities which include, but are not limited to:
+ Analysis and assessment of Critical Cases, including SUSARs
+ Detection of single case potential safety signals/ through validation
o Identification and analysis of new safety signals and trends by conducting systematic reviews of aggregate data.
o Review local literature for potential signals assessed by vendors and Local Management Safety (LMS)
+ Active participation in Signal Evaluation
+ Ensuring Follow-up of all critical case/ Events of Special Interest (RMPs identified risks)
+ PBRER/PADER activities
+ Investigator Brochure activities
+ Watchlist/TFUQ activities
+ Vendor oversight activities as assigned
o Additional ad hoc activities that may require physician input, examples:
+ Standard Operating Procedures (SOPs)
+ CAPAs
+ Audits/inspection activities
· Participation in pharmacovigilance matrix-teams (i.e. Safety Management Teams) responsible for pharmacovigilance activities focused on products and therapeutic areas as assigned.
· Support GMS Product Team to drive change, increase efficiency, effectiveness and quality, and foster alignment, across GMS and with key stakeholders.
+ undefined
· Lead cross functional projects/teams, as assigned.
**Minimum Qualification**
+ Physician (MD or equivalent) with a medical degree from a recognized medical institution.
+ A minimum of 1 year of clinical practice after postgraduate training program is preferred.
+ A minimum of 3 years of experience in industry, academia, or patient care settings is required.
+ Direct experience in pharmacovigilance is strongly preferred.
+ Experience and knowledge of Good Clinical Practices is strongly preferred.
+ Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers.
+ Fluent in written and spoken English.
+ Working knowledge of the use of Microsoft suite of software products, including Excel and Word.
**Required Skills:**
**Preferred Skills:**
Clinical Operations, Compliance Management, Compliance Risk, Critical Thinking, Cross-Functional Collaboration, Medicines and Device Development and Regulation, Organizing, Quality Control (QC), Research Ethics, Risk Management, Risk Management Framework, Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Tactical Planning, Team Management
**The anticipated base pay range for this position is:**
50,500.00 - 86,365.00
**Benefits:**
In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees' and companies' performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location's eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers. ( is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
**Additional information:**
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.

**General Description:**
The Regional Clinical Compliance Lead is responsible for leading, developing, and managing a team of Clinical
Compliance professionals supporting country- and site-level oversight. This role combines people leadership with
operational and strategic accountability to ensure consistent, high-quality execution of risk-based compliance
activities.
This role plays a critical role in building team capability, driving performance, and ensuring alignment with global
compliance strategies while fostering a culture of quality, accountability, and continuous improvement.
**Essential Functions**
- Serve as the primary point of contact for the RCC country compliance managers team regarding: - GCP requirements
- Company and study-specific procedures
- General compliance-related queries
- Provide expert guidance and interpretation of regulations and internal standards to ensure consistent and compliant practices.
- Oversee preparation, execution, and follow-up activities for inspections
- Provide leadership support during high-impact audits and inspections.
- Ensure consistent application of lessons learned across the team.
_Operational Oversight & Execution Excellence_
- Ensure consistent and high-quality execution of risk-based compliance activities across countries and studies.
- Monitor key performance indicators (KPIs), quality metrics, and compliance trends across the team-
Identify systemic risks, recurring issues, and areas for improvement.
- Ensure timely escalation to Head RCC EMEA and effective resolution of critical compliance issues.- Drive accountability for CAPA quality and effectiveness.
- Provide oversight and quality review of:
- Remote Compliance Activities
- Risk identification and mitigation strategies
- Site-level compliance assessments
- Drive standardization and harmonization of processes across the team.
_Resource & Capacity Management_
- Manage and oversee the budget, resource allocation and workload balancing across the team based on
study portfolio and risk profile.
- Ensure appropriate resourcing for high-risk studies, sites, and compliance activities.
- Partner with senior leadership on workforce planning and capability needs.
_Strategic Alignment & Cross-Functional Partnership_
- Translate global compliance strategies into clear team-level objectives and actions.
- Ensure alignment between local execution and global expectations by partnering with:
- RCC Inspection and Audit Lead
- RCC Process Excellence and Risk Surveillance
- Global Clinical Compliance
- Clinical Operations leadership
- Quality Assurance teams
- Represent the function in governance forums and cross-functional discussions.
_Core Competencies, Knowledge and Skill Requirements:_
- Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated
regulatory guidelines
- Analytical and problem-solving skills
- High attention to detail and quality orientation
- Excellent communication and stakeholder management skills
_Communication & Interpersonal Skills:_
- Excellent English written and verbal communication and interpersonal skills
- Excellent organizational skills and ability to prioritize and multi-task
- Ability to work independently in multi-cultural setting and effectively handle multiple priorities in a fast-paced environment
_Supervisory Responsibilities:_
- Lead, coach, and develop a team of Regional Clinical Compliance professionals across multiple countries.
- Set clear performance expectations and conduct regular performance reviews (goal setting, mid-year,
year-end).
- Build organizational capability by identifying skill gaps and implementing targeted development plans.
- Foster a culture of quality, accountability, continuous improvement, and psychological safety.
- Drive talent management, including succession planning and retention of key talent.
- Promote an inclusive, collaborative, and high-performing team environment aligned with company values.
- Encourage feedback, innovation, and continuous learning.
- Model ethical behavior and reinforce a compliance mindset across the team
**Qualifications**
-Bachelor's degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with minimum of 8 years of progressive experience in clinical operations roles plus minimum 6 years' experience in a GCP compliance or equivalent role (i.e. quality) **including people management experience (minimum 4 years).**
- Experience in oncology global trials is preferred.
- Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
- Sound working knowledge of relevant terminology, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), applicable regulatory requirements, quality management processes.
- Excellent organizational, interpersonal and communication skills.
- Excellent judgement and decision-making skills.
- Demonstrated leadership and line management skills.
- Excellent influencing and negotiation skills.
- Strong computer skills including Microsoft Office applications.
- Excellent problem-solving skills.
- Demonstrated ability to work in a matrix environment.
- Ability to lead and motivate a clinical team also required.
- Ability to travel within the region/country.
- Ability to establish and maintain effective working relationships with co-workers, managers and clients.
- Fluent in English.
**Please note: this role is not eligible for UK VISA sponsorship.**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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