Associate Medical Director - Oncology/Hematology

November 11

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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

• Provides medical oversight of clinical trials to ensure compliance with regulations and guidelines. • Attends investigator and sponsor meetings, provides medical consultation to clients and project team. • Reviews clinical trial serious adverse events, marketed products ICSR, and safety reports. • Ensures adherence to regulations and ICH guidelines regarding clinical trials and safety issues. • Provides medical consultation to team members and answers study-related medical questions. • Contributes to process improvement initiatives in the department.

Requirements

• MD or equivalent required. • Active medical licensure preferred. • Clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (comparable to 2 years); • Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; • Direct experience in safety/Pharmacovigilance (comparable to 2 years). • Clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (comparable to 2 years) and one of the following: Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; • Direct experience in safety/Pharmacovigilance (comparable to 2 years). • Qualified candidates should have a background as a formally trained oncologist and/or hematologist with clinical experience. • 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.