 Location: Kochi, Thane, Pune, Kolkata, Bangalore (Hybrid Mode)
Experience: 3 – 5 years
Company: Clinovo
About Us: At Clinovo, we’re committed to accelerating clinical trials globally. Our mission is to drive innovation and efficiency in clinical research, ensuring the highest standards of safety and efficacy in the development of new treatments.
Role Overview: We are seeking a skilled Pharmacovigilance Specialist to join our dynamic team. The ideal candidate will have a strong background in pharmacovigilance and be adept at managing case processing, quality reviews, and ensuring compliance with Good Pharmacovigilance Practices (GVP).
Key Responsibilities:
- Case Processing: Manage and process individual case safety reports (ICSRs) in Argus and other safety databases.
- Legal Case Processing: Handle legal case processing activities as required.
- Quality Review: Conduct quality reviews to ensure accuracy and compliance with regulatory requirements.
- GVP Compliance: Ensure adherence to Good Pharmacovigilance Practices (GVP) and internal standards.
Skills Required:
- Proficiency in Argus and other pharmacovigilance software.
- Strong experience in case processing and quality review.
- Knowledge of GVP and regulatory guidelines.
- Excellent analytical and communication skills.
Why Join Us?
- Work with a global leader in clinical trial acceleration.
- Enjoy the flexibility of a hybrid work model.
- Be part of a collaborative and forward-thinking team.
How to Apply: If you are passionate about pharmacovigilance and meet the qualifications, we would love to hear from you! Please send your resume to bhavanasri.gundala@clinovo.com.
Clinovo is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
