Teva Hiring Clinical Research Asscoiate [B.Pharm, M.Pharm, Msc, BSc]

How You’ll Spend Your Day:

• Staff Management:
  • Ensure availability of sufficient, qualified, trained, and experienced staff.
  • Train staff on SOPs, revised SOPs, and protocols before activity commencement.
  • Ensure all activities comply with SOPs and protocols.
• Instrument Management:
  • Ensure all instruments are calibrated as per the schedule in coordination with the GLP engineer.
• Coordination:
  • Coordinate with Pathology Lab, QA department, statistician, accounts department, and other concerned departments for the smooth execution of clinical studies.
• Document Review:
  • Review study documents to ensure adherence to SOPs and regulatory requirements.
• Document Preparation:
  • Prepare and review study documents such as e-CRF, study plan, study updates, clinical tables, SDTM, etc.
• Maintenance:
  • Responsible for the maintenance of ICU and cardiac ambulance, including inventory and calibration of instruments.

Application Link