Review and processing serious adverse events, spontaneously reported adverse reactions and/or other medically related project information such as adverse events of special interest and clinical endpoints.
Ensuring all RPL, Sponsor and regulatory timeframes are met for the processing and reporting of safety information.
Assisting in ensuring the completion of all departmental project activities accurately in accordance with RPL SOPs, study operating manuals, regulatory requirements, and contractual obligations to Sponsors/Sponsor processes.
Providing input and review relevant safety tracking systems for accuracy and quality.
Ensuring Good Documentation Practice and all documentation pertaining to safety are maintained in the project files
Performing safety review of clinical and diagnostic data
Liaising with Sponsor and internal departments as necessary for issues related to safety including attending internal and client meetings as required
Job Types: Full-time, Fresher
Salary: ₹15,000.00 – ₹25,000.00 per month
Benefits:
- Internet reimbursement
Schedule:
Supplemental Pay:
- Performance bonus
Work Remotely:
के लिए आवेदन देना Pharmacovigilance Associate – Qualex research – Hyderabad, Telangana.
नौकरी रिक्ति Pharmacovigilance Associate – Qualex research – Hyderabad, Telangana तथा Pharmacovigilance Associate – Qualex research – Hyderabad, Telangana वेतन.