...This is a full-time on-site role in Bengaluru for a Drug Safety Associate. The Drug Safety Associate will be responsible for tasks such as
~ Reviewing safety data, writing narratives, performing quality control ch...
...responsibility of this position relies on Managing the Department including coaching/mentoring/training/support of direct reports and development plan... .... An educational background as a B...
...Summarized Purpose:
Responsible for the planning, coordination and delivery of safety writing services for multiple clinical trial and/or marketed product projects. Performs day-to-day safety writing and related ...
...Key Responsibilities (includes and not limited to)1.Product or Molecule Safety Physician / Lead Physician
a) Provide global medical leadership and input into all aspects of safety of assigned product(s) including...
...procedures
Conduct risk-benefit assessments of pharmaceutical products
Stay up-to-date on the latest pharmacovigilance regulations and guidance
Qualifications
~ Bachelor's degree in a related field, such ...
...Job Title: Associate Medical Director, Senior Patient Safety Physician
Career Level: E
Introduction to role:
The Associate Medical Director, Senior Patient Safety Physician independently or in association w...
...Job Description :
1) Should be a medical doctor - preferably with MD in Pharmacology
2) 4+ years- experience in handling Phase 2/Phase 3 clinical trials in India
3) Manage the CRO team for all clinical ...
Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company representatives
Assess the severit...
The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review, writing signal detection reports, supporting writing and or reviewing of aggregate reports (DSURS, PSURS, PBRERs, PADERS).
To review and app...
...Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company rep...
