Dr. Reddy’s Laboratories is hiring a Clinical Research Associate for their Hyderabad location. This full-time, on-site role involves various responsibilities related to clinical trial management, including site qualification visits, data management, monitoring, and compliance with Good Clinical Practice (GCP) and regulatory requirements.
Key Responsibilities:
- Facilitate study start-up activities and conduct feasibility assessments.
- Manage investigational sites, ensuring they are equipped and trained for trial activities.
- Coordinate clinical trial materials, ensure site documentation, and manage IP accountability.
- Review and resolve data issues in collaboration with internal teams (e.g., Data Management, Safety, Medical).
- Ensure compliance with protocols, SOPs, GCP, and other regulatory guidelines.
- Maintain Trial Master Files (TMF) for inspection readiness.
Qualifications:
- Master’s degree in Pharmacy, Life Sciences, Biology, Biotechnology, or Biochemistry, or a Diploma in Clinical Research.
- 2-5 years of clinical research experience.
- Proficiency in EDC systems, regulatory guidelines (GCP, ICH), and MS Office.
Skills:
- Strong communication, project management, and analytical abilities.
- Knowledge of pharmacovigilance and clinical trial operations.
Benefits:
- Personalized learning programs, family support (maternity/paternity), medical and life coverage.
For more details, visit the Dr. Reddy’s career website.