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 medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
A day in the Life :
* Provide medical leadership to study teams, including creating clinical trial protocols, implementing the latest scientific information, contributing to site selection, and reviewing and approving study protocols, amendments, CSRs, ICFs, CRFs, protocol deviations, and other clinical documents.
* Real-time Medical Monitoring of clinical studies to ensure medical validity of primary endpoints and subject safety, identifying issues early, and consulting with the Global Medical Indication Lead for corrective actions.
* Review protocols, support staff regarding procedural and budgetary items, and address changes due to amendments. Serve as liaison between sponsor and internal departments, and educate investigators and site staff through meetings and presentations.
* Act as medical point of contact for stakeholders, interact with investigators, answer IRB and Health Authority questions, and ensure compliance with SOPs and GCP.
* Collaborate with study team members to clarify medical risks, issues, and results.
Education :
* MD, MB / BS or equivalent with strong medical knowledge and clinical experience, especially in Neurology.
Knowledge, Skills, Abilities :
* Extensive experience in the pharmaceutical industry, clinical trials, and pharmaceutical medicine.
* Fluent in spoken and written English.
* Understanding of NDA submission process and regulatory guidelines for adverse event reporting.
* Excellent communication, presentation skills, and team collaboration.
Apply today!
Thermo Fisher Scientific is an EEO / Affirmative Action Employer and does not discriminate on any protected basis.
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