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.
Discover Impactful Work: The (Associate) Medical Director will provide medical support and advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
A day in the Life :
1. Provide medical leadership to study teams, including creating clinical trial protocols while implementing the latest scientific information.
2. Contribute to site selection, review, and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions, and other clinical documents as required for the conduct of clinical trials.
3. Ensure real-time medical monitoring of clinical studies to validate primary endpoints and ensure participant safety, identifying medical issues early.
4. Proactively address customer concerns and correct issues in consultation with the Global Medical Indication Lead.
5. During initial protocol review, consult with internal groups and support staff regarding procedural and budgetary considerations, and adapt to protocol amendments as needed.
6. Collaborate with other functions to close gaps and address issues promptly and effectively.
7. Serve as the primary liaison between the sponsor and all internal PPD departments during all study phases.
8. Educate investigator sites through protocol-specific lab procedures presentations and demonstrations during investigator meetings.
9. Manage day-to-day activities during clinical trials, resolving issues and answering queries.
10. Act as the medical point of contact for internal and external stakeholders: interact with investigators, respond to IRBs and Health Authorities, prepare and present materials to study committees, and provide medical training at investigator meetings and for CRAs in new indications.
11. Ensure compliance with all medical aspects of the study by understanding and applying relevant SOPs and GCP guidelines.
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