Company Description

• Freshers (0-1 Year) only and Education in M Pharmacy 2020/2021/2022 Passouts only.

• Work under Clinical Research Managers/Principal Investigators, tasked with administering clinical trials.
• Primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.

• Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.
• Documentation and recording of information through computerized processes such as clinical trial management systems and electronic data capture.
• Liaising with doctors/consultants or investigators on conducting the trial.
• Setting up the trial sites, which includes ensuring each center has the trial materials, including the trial drug often known as the investigational medicinal product. Source data verification.
• Monitoring the trial throughout a specified duration involves monitoring visits to the trial sites.
• Informed consent form review, case report form review, investigational drug accountability, and adverse event review. Ensuring all unused trial supplies are accounted.
• Writing visit reports, filing and collecting trial documentation and reports.

• Excellent communication skills (both written and oral)
• Education must be in M Pharmacy 2020/2021/2022 Passouts only.
• Candidate must be trained in any Research Institute/Hospital Research at least (on Clinical Research) 6months.