Pharmacovigilance Job at Parexel, Hyderabad
Want to start or grow your career in pharmacovigilance and drug safety? Parexel is hiring a Patient Safety Associate II in Mohali and Hyderabad. This Pharmacovigilance Job at Parexel Careers in Hyderabad focuses on global safety operations, including case processing and reporting. You will support clinical trials and post-marketing safety activities. It is ideal for candidates with experience in pharmacovigilance and life sciences. The position offers exposure to global regulatory and safety systems.
About the Company:
Parexel is a leading global Clinical Research Organization (CRO) specializing in clinical trials, regulatory consulting, and pharmacovigilance services. The company collaborates with pharmaceutical and biotechnology clients to accelerate drug development and ensure patient safety across global markets.
Job Details:
- Job Role: Patient Safety Associate II
- Location: Mohali / Hyderabad
- Job ID: R0000039131
- Category: Medical Sciences
- Work Type: On-site / Hybrid (as per project)
- Experience Required: Minimum 2 years in Pharmacovigilance
Key Responsibilities:
- Perform Individual Case Safety Report (ICSR) processing and data entry
- Monitor and review safety reports from multiple sources
- Ensure MedDRA coding and case documentation accuracy
- Support regulatory submissions and compliance tracking in this Pharmacovigilance Job in Hyderabad
- Conduct a literature search and review for safety signals
- Assist in safety data reconciliation and quality checks at Parexel Careers
- Collaborate with global teams and affiliates
- Support audits, inspections, and process improvements
- Maintain documentation and ensure adherence to regulatory guidelines
Educational Requirements for this Job:
- Degree in Pharmacy
- Equivalent qualification or relevant work experience may be considered
Skills Required:
- Basic knowledge of pharmacovigilance and drug safety processes
- Understanding of ICH guidelines and regulatory requirements
- Good communication and teamwork skills
- Analytical thinking and problem-solving ability
- Organizational and time management skills
- Familiarity with safety databases and MS Office tools
Benefits of the Job:
- Opportunity to work in global pharmacovigilance projects
- Exposure to international safety reporting systems
- Career growth in clinical research and drug safety
- Collaborative and learning-focused work environment
- Hands-on experience with regulatory compliance and safety databases
