TRABAJO DRUG SAFETY PHYSICIAN

Prepares safety data for health authority review boards... experience in preparing or contributing to the preparation of clinical safety assessments and regulatory...

Experience (years/area): at least 4 years of experience in pharmacovigilance and drug safety... ready to be a #challenger?what are we looking for? ?as a member of...

The senior manager, safety scientist in collaboration with medical directors, global drug safety are responsible for safety surveillance and risk management activities...

At the drug screening platform (dsp), we support chemical biology and drug discovery projects... good working conditions: permanent contract (científico técnico)...

They are urgently seeking a clinical research physician (director / sd level) to join their clinical development team... provide scientific leadership by staying...

Periodic safety update reports (psurs), drug safety update reports (dsurs), and other safety related documents) in collaboration with patient safety may be assigned...

Minimum 5 years in pharmacovigilance, with solid understanding of epidemiology, drug safety regulations, and benefit-risk assessment methodologies... com/us/en/workplace-accommodation)...

Investigator’s brochures, health authority briefing books, safety updates, submission dossiers, and responses to health authorities) in collaboration with appropriate...

Tasks and time per task contracted) and according to the assigned role (global lead physician or regional lead physician)... the medical director is a medical expert...

Good knowledge of the drug development process... plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction)...

Clinical practice experience (including residency/fellowship) and board certification or eligibility in nephrology experience in clinical research or drug development...

Desirable   experience with regulatory submissions, life cycle management, advisory boards, annual safety updates...     the global development scientist associate...

Desirable experience with regulatory submissions, life cycle management, advisory boards, annual safety updates... the global development scientist associate director/director...

safety this position will adhere to safety rules, practices, and training as outlined in all borgwarner safety policies and procedures...

Disseminate drug information either verbally or by written correspondence... the utilization of medical information management systems, safety databases, or equivalent...

Prove out safety and functionality... any offer of employment is conditioned upon the successful completion of a drug screen (as applicable)... is a “sponsor”)...

Cdm will lead and contribute to data management activities in support of client's studies across all stages of clinical drug development... summary of key responsibilities...