Associate Medical Director - Oncology/Hematology

November 11

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Thermo Fisher Scientific

Analytical Instruments β€’ Laboratory Supply Chain Programs and eCommerce β€’ Laboratory Equipment β€’ Lab Services β€’ Specialty Diagnostics

Description

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

Requirements

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

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