Associate Medical Director - Neurology

October 29

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Thermo Fisher Scientific

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Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics

10,000+

Description

• Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in 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. • Real time 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. • Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead. • Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. • Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries. • 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; medical training of site staff at Investigator meetings; CRA training in new indications. • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP. • Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties.

Requirements

• MD, MB/BS or equivalent degree and strong medical knowledge • Shown clinical experience running Neurology patients in clinical and/or hospital practice. • Experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important. • Is fluent in spoken and written English. • Shown understanding and experience with NDA submission process. • Shown understanding of regulatory guidelines for adverse event reporting. • Strong communication & presentation skills and is a strong teammate.