Entry-level Clinical Research Jobs | Medpace Hiring | Apply Online
Looking for exciting Clinical Research Jobs in India? Medpace Careers has announced an excellent opportunity for aspiring professionals through its Clinical Research Associate (CRA) Entry position in Navi Mumbai. This opportunity is ideal for candidates from Life Sciences Jobs backgrounds who want to build a rewarding career in clinical research, clinical trials, and drug development. With Medpace’s renowned PACE® training program, even candidates without prior research experience can gain the skills needed to succeed in the clinical research industry.
- Job Title: Clinical Research Associate (CRA) Entry
- Job ID: 12794
- Location: Navi Mumbai, India
About the Company
Medpace is a leading full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, the company operates across nearly 40 countries and employs thousands of professionals worldwide. Medpace focuses on accelerating the development of safe and effective medical therapies through scientific expertise and regulatory excellence. The organization is recognized for its strong training culture, career growth opportunities, and commitment to advancing global healthcare.
Key Responsibilities
- 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.
Qualifications
- Minimum of a bachelor’s degree in Life Sciences related field preferred.
- Candidate with Clinical Research Coordinator experience is an advantage.
Skills Required
- Good communication and presentation skills.
- Understanding of healthcare and clinical research concepts.
- Knowledge of Microsoft Office.
- Strong documentation and analytical abilities.
- Willingness to travel approximately 60–80% nationally.
- Attention to detail and problem-solving skills.
For candidates seeking Clinical Research Jobs with a globally recognized CRO, this opportunity through Medpace Careers offers an excellent pathway into the clinical research industry. The structured training, exposure to multiple therapeutic areas, and strong career advancement opportunities make this one of the most attractive Life Sciences Jobs currently available for graduates and early-career professionals. Interested candidates should submit their applications at the earliest opportunity.
