Medpace Hiring Clinical Research Associate Entry | Navi Mumbai

Clinical Research Associate Entry

Medpace is seeking entry-level Clinical Research Associates with backgrounds in medical or life science related fields. Individuals who have succeeded in this role have come from professions such as nursing, dietetics, pharmacy technology, pharmaceutical or device sales, biotech engineering, health and wellness coordination, research assistance, and advanced life science programs.

PACE Training Program

No prior research experience is required. Medpace provides extensive initial and ongoing training through the PACE training program. This program helps new associates build the skills required to perform CRA responsibilities effectively and progress toward becoming an independent clinical research professional.

• The program equips new hires with practical knowledge and confidence to perform monitoring duties.
• Training includes interactive discussions, hands-on exercises, and job related practicums designed to strengthen CRA capabilities.
• Participants may also rotate across clinical research departments to learn additional aspects of the drug and medical device development process.

Role Overview

This position offers a dynamic environment with varied responsibilities and exposure to multiple therapeutic areas. Clinical Research Associates work alongside regulatory and therapeutic specialists while contributing to the advancement of pharmaceutical and medical device research.

• Work in a collaborative environment with experienced regulatory and therapeutic experts.
• Gain exposure to several therapeutic areas and clinical development processes.
• Follow a defined career path with opportunities for advancement, mentoring, and leadership roles.
• Receive competitive compensation along with travel related incentives.

Key Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites while ensuring compliance with approved study protocols.
• Communicate regularly with medical site personnel including coordinators, investigators, and clinical research physicians.
• Confirm that investigators have appropriate qualifications, training, facilities, laboratory access, equipment, and staff support.
• Review medical records and source documentation against case report form data while ensuring proper documentation practices and reporting protocol deviations in line with SOPs, GCP, and regulatory requirements.
• Verify that investigators enroll only eligible study participants according to protocol requirements.
• Review regulatory documentation and ensure study documentation remains accurate and complete.
• Track investigational products or medical devices, including accountability and inventory management.
• Evaluate and verify reporting of adverse events, serious adverse events, and related medical data for accurate protocol compliance.
• Assess patient recruitment and retention at research sites and recommend improvements when needed.
• Prepare monitoring reports and follow-up letters summarizing key findings, deviations, deficiencies, and recommended corrective actions.

About Medpace

Medpace is a global clinical contract research organization providing Phase I to Phase IV clinical development services for biotechnology, pharmaceutical, and medical device companies. The organization focuses on accelerating the development of safe and effective therapies through a scientific and disciplined approach.

Headquartered in Cincinnati, Ohio, Medpace employs more than 4,000 professionals across nearly 40 countries and supports research across therapeutic areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system disorders, and infectious diseases.

Company Benefits

• Flexible working environment.
• Comprehensive compensation and benefits package.
• Competitive paid time off policies.
• Structured career progression with opportunities for professional development.
• Employee appreciation programs and wellness initiatives.

Over the past three decades, Medpace has contributed to research that has positively impacted patients and families across many disease areas. The organization continues to support the development of treatments that improve health outcomes worldwide.