Location– Bangalore
Education
- Registered nurse/pharmacist or with health/biomedical degree or other related scientific degree/qualification is required.
- Postgraduate qualifications or certification in clinical trials will be an advantage.
Knowledge, Skills, and Abilities (Pharmacovigilance Associate)
- Knowledge of clinical trials and pharmacovigilance requirements. Knowledge/experience in international drug safety-regulatory reporting obligations and compliance.
- Experience in coding medical terminologies, case processing, safety report submission is preferred.
- Thorough knowledge of medical terminology and ability to summarise medical information is required.
- Strong computer proficiency and ability to work in specific databases is required/preferred.
- Ability to follow guidelines and procedural documents is required. Experience of working with SOPs etc. is required.
- Fluent in both written and oral English.
- Good interpersonal skill to professionally communicate with all levels of the organizations.
- Good time management & multi-task capability.
Experiences
- 2 years to 4 years of pharmaceutical/CRO experience with focus on safety related areas in clinical trial is required.
