• 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