(Associate) Medical Director - Endocrinology (Client-Dedicated), EMEA

Thermo Fisher Scientific; Madrid; Presencial; EUR 80.000 - 120.000; Jornada completa

Descripción de la vacante

An established industry player seeks a dedicated Endocrinologist Medical Director to lead clinical trials and ensure adherence to regulatory standards. This role involves providing medical oversight, creating clinical trial protocols, and collaborating with study teams to enhance patient outcomes. In a dynamic environment, you will liaise with investigators and stakeholders, ensuring the safety and efficacy of treatments. Join a mission-driven organization that values integrity and innovation, where your expertise will directly impact global health and contribute to life-changing therapies. This is an exceptional opportunity to make a difference in the field of medicine.

Formación

• MD degree or equivalent board certified in Endocrinology required.
• 4+ years relevant experience in clinical development or pharmacovigilance.

Responsabilidades

• Provide medical leadership and oversight of clinical trials.
• Ensure compliance with SOPs, GCP, and regulatory requirements.
• Act as medical point of contact for internal and external stakeholders.

Conocimientos

Medical Leadership

Clinical Trial Protocols

Medical Monitoring

Communication Skills

Team Collaboration

Fluency in English

Educación

MD degree in Endocrinology

Active medical licensure

4+ years in clinical development

5+ years medical experience as Endocrinologist

Descripción del empleo

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 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.

Discover Impactful Work:

The Endocrinologist Medical Director provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities.

A Day in the Life:

1. Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information.
2. Contribute to site selection through feasibility support.
3. Involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), protocol deviation decisions and other documents requiring medical input.
4. Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early.
5. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead.
6. Serve as chief medical liaison between sponsor and all PPD internal departments performing the required tasks during all study phases.
7. Liaise with Investigator sites by delivering protocol specific advice on subject eligibility, protocol clarifications and safety concerns, lab procedures presentation and demonstration during an investigator meeting.
8. Act as medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; provide medical training of site staff at Investigator meetings; CRA training in new indications.
9. Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP.
10. Closely collaborate with the cross functional study team members for medical risks, issues, and results to be clear to all involved parties.

Education:

1. MD degree or equivalent board certified in Endocrinology.
2. Active medical licensure (preferably in country of residence).
3. 4+ years relevant experience such as pharmaceutical industry or CRO, in clinical development or pharmacovigilance or significant clinical trial experience as a principal investigator.
4. 5+ years medical experience as an Endocrinologist treating physician.
5. Previous experience with cell-therapy or gene therapy.

Knowledge, Skills, Abilities:

1. Experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is considered beneficial.
2. Experience from treatment of Graves disease would be an advantage.
3. Fluent in spoken and written English.
4. A team player.

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.