Hiring Clinical Research Associate at Medpace

Corporate activities are growing rapidly, and we are currently seeking a full-time, office-based RSP (Randomization & Study Product) Coordinator to join our team in India. By working with the other RSPM team members, these professionals ensure the accuracy of RSPM system data, as well as assisting in the management of study product for studies. If you are detail-oriented and enjoy an adaptive, challenging work environment, this could be the opportunity for you. This is an entry level role. As new hires, RSPM Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field.

Post : Clinical Research Associate Entry

Job Summary
Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:
• Nurses
• Dieticians
• Pharmacy Technicians
• Pharmaceutical/Device Sales Representatives
• Biotech Engineers
• PhD/Pharm.D candidates
• Health and Wellness Coordinators
• Research Assistants.

Job Description
As a CRA Entry, you will specifically be responsible for the following:
• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Candidate Profile
• Minimum of a bachelor’s degree; Health or life science related field preferred;
• Candidate with Clinical Research Coordinator experience is an advantage:
• Willing to travel approximately 60-80% nationally;
• Familiarity with Microsoft® Office; and
• Strong communication and presentation skills a plus.

Additional Information
Qualification : Minimum of a bachelor’s degree
Location : Navi Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Research
End Date : 10th October 2026