Overview
Job Description
We are seeking a full-time, office-based Clinical Research Project Coordinator for our Clinical Trial Management team in Navi Mumbai, India. This position involves working collaboratively to achieve tasks and projects crucial to the company's success. This is an opportunity to leverage your existing expertise and further develop your career.
Responsibilities
- Engage in day-to-day clinical trial management activities.
- Work closely with the project Clinical Trial Manager (CTM) to ensure timely and accurate delivery of recurring tasks.
- Compile and maintain project-specific status reports.
- Update the Clinical Trial Management System (CTMS) with study milestones, enrollment projections, and other relevant data.
- Update the electronic Trial Master File (eTMF) and perform ongoing eTMF quality control.
- Support the Clinical Trial Manager in drafting study plans and specific guidance documents.
- Manage site feasibility, site activation preparation, and study supply management.
- Communicate effectively with regional cross-functional teams, vendors, and sponsors.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through advanced clinical research. We utilize in-country regulatory and therapeutic expertise across major therapeutic areas, including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ over 6,500 individuals across more than 40 countries.
Why Medpace?
Joining Medpace means becoming part of an innovative team dedicated to bringing cutting-edge therapies to market. You will build a meaningful and rewarding career focused on scientific excellence and improving patient outcomes globally through continuous learning and cross-functional collaboration.
Purpose-Driven Work
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
Collaborative Culture
- Contribute to an interactive team environment that fosters decision-making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership at Medpace is both accessible and approachable.
Continuous Growth & Development
- Benefit from an office-based environment with on-site mentors.
- Follow defined career paths with clear advancement opportunities.
- Participate in industry-renowned onboarding and training programs designed to accelerate professional development.
- Access ongoing training and continuous learning opportunities throughout your career.
- Work in an environment that encourages employees to influence change, contribute ideas, and grow quickly.
Other Employee Benefits
- Competitive compensation programs that recognize and reward performance.
- Comprehensive health, wellness, retirement, and Paid Time Off (PTO) benefits.
- An office-based culture with occasional work-from-home options, providing flexibility for eligible positions after training.
- Company-sponsored social events.
Please note that benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application. If your profile matches our current needs, you will be contacted for an interview. While we carefully review all applications, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
If an employer asks you to pay any kind of fee, please notify us immediately. Talentd does not charge any fee from applicants and we do not allow other companies to do so.
Key Skills
Related Tags
Education Requirements
- Bachelor's degree in a life sciences field
Eligible Batch Years

Medpace
Medpace is a global, full-service clinical contract research organization (CRO) headquartered in Cincinnati, Ohio, USA. Founded in 1992, the company specializes in providing comprehensive development services to the biotechnology, pharmaceutical, and medical device industries. Medpace's mission is to accelerate the development of safe and effective medical treatments through scientifically-driven, high-quality clinical research. With a focus on therapeutic areas such as oncology, cardiology, metabolic disease, and infectious disease, Medpace offers expertise across all phases of clinical trials.
Employing over 5,000 professionals worldwide, Medpace has built a strong reputation for its integrated approach, combining regulatory, medical, and operational expertise to deliver efficient and reliable results. The company operates in multiple countries, enabling it to manage global trials with localized knowledge. In recent years, Medpace has reported steady growth and strong financial performance, reflecting increasing demand for outsourced clinical research services. Its commitment to quality and scientific rigor has positioned it as a trusted partner for sponsors seeking to bring innovative therapies to market.
Company Details
Connect With Us
Websitemedpace.com