Nursing

Your focus will be on coordinating pharmacovigilance and drug safety delivery, resolving issues, and developing team capability.

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs.

As a Patient Safety Associate II/Specialist, you will support global pharmacovigilance activities that advance new treatments for patients. This position plays a key role in safety case processing, regulatory submissions, literature surveillance, and compliance with international regulations.

PGs, PharmD, MPharm Pharmacology/Pharmacy Practice with some experience in clinical research and other Life Sciences PG degrees with clinical research experience. Division of Clinical Pharmacology, Department of Pharmacology, Kasturba Medical College (KMC), Manipal.

Provide support to Ergomed colleagues and functional teams in developing, managing, and implementing Controlled Procedures. 

The Senior Pharmacovigilance Safety Scientist, Benefit Risk is expected to be professional and diligent and liaise with the director and management group members within the team on any issues, as well as coordinate the work with the senior PV Scientists. Pharma, Life Science candidates to Join ProPharma

Minimum second class or equivalent CGPA with four- year Bachelors degree in Pharmacy (B. Pharm). First class Post Graduate Degree, including the integrated PG degree in Microbiology/Biochemistry, Genetics/Immunology. Government Medical College and Hospital, Chandigarh

Data entry of safety data onto adverse event database and tracking systems.Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.

Office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.