- Assist in the planning, execution, and management of clinical trials.
- Ensure that the trial is conducted in compliance with the protocol, SOPs, and regulatory requirements.
- Monitor clinical sites to ensure proper study conduct.
- Maintain accurate and complete records of all trial-related activities.
- Communicate effectively with clinical sites, sponsors, and other stakeholders.
Qualifications and Experience:
- Education: B. Pharm, M. Pharm preferred. A Post Graduate Diploma in Clinical Research is a plus.
- Skills: Strong understanding of clinical trial processes, excellent organizational skills, and attention to detail.
- Preferred: Candidates who can commute to IDC, M. G. Road, Sector 16, Gurgaon.
If you are interested and meet the qualifications, please send your resume to rashiofficesharma@gmail.com
