Medical Director - Neurosciences

October 29

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Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

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

10,000+

Description

β€’ Provides medical oversight of clinical trials. β€’ Attends and presents at investigator and sponsor meetings. β€’ Provides medical consultation to clients, investigators and project team members. β€’ Supports business development activities. β€’ Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle. β€’ Ensures tasks delegated to PVG are properly executed. β€’ Adheres to applicable regulations and ICH guidelines regarding clinical trials. β€’ Communicates clearly with associates and clients. β€’ Provides therapeutic training and protocol training on assigned studies. β€’ Contributes to departmental process improvement initiatives. β€’ Monitors all safety variables of clinical studies. β€’ Discusses all medical concerns with principal investigators and clients. β€’ Performs data review as specified in the client contract and data validation manual.

Requirements

β€’ MD or equivalent required. β€’ Active medical licensure preferred. β€’ Board certified or eligible. β€’ Candidates should have a combination of clinical experience and industry experience. β€’ Therapeutic expertise across one or more medical specialty or sub-specialties. β€’ Strong decision-making, problem solving, organizational skills and analytical skills. β€’ Excellent oral and written communication skills. β€’ Working knowledge of relevant safety databases (e.g. Medra). β€’ Flexibility to travel domestically and internationally. β€’ Ability to work independently, analyze work with attention to detail, process and prioritize sensitive complex information. β€’ Proficiency in basic computer applications. β€’ Fluent in spoken and written English. β€’ Excellent interpersonal, influencing and team building skills. β€’ Understanding guidelines (FDA, ICH, EMA and GCP). β€’ Working knowledge of biostatistics, data management, and clinical operations procedures. β€’ Ability to act as a mentor/trainer to other staff within PVG. β€’ Additional experience is required for Sr Med Director level.

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