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Experienced Clinical Research Associate

Medpace
2-4 years
₹8–15 LPA
Mumbai, Navi Mumbai, India
15 June 24, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Experienced Clinical Research Associate (CRA)

Company: Medpace
Job Title: Experienced Clinical Research Associate (CRA)
Job ID: 12793
Location: Navi Mumbai, India

Salary: ₹8–15 LPA (Estimated for candidates with 2–4 years of CRA experience; final compensation depends on experience, therapeutic expertise, and interview performance)


Job Summary

Medpace is seeking experienced Clinical Research Associates to support clinical trials across multiple therapeutic areas. Selected candidates will receive ongoing professional development through Medpace's PACE® (Professionals Achieving CRA Excellence) Training Program while contributing to the successful execution of clinical studies.

Professionals who have successfully transitioned into CRA roles include:

  • Nurses

  • Dieticians

  • Pharmacy Technicians

  • Pharmaceutical/Medical Device Sales Representatives

  • Biotechnology Engineers

  • PhD/Pharm.D Candidates

  • Health & Wellness Coordinators

  • Research Assistants


PACE® CRA Training Program

The Medpace PACE® Program offers:

  • Continuous CRA development and advanced training

  • Interactive discussions and practical learning exercises

  • Hands-on field and in-house training

  • Exposure to multiple aspects of clinical research and drug development

  • Opportunities to enhance monitoring and regulatory expertise


Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and closeout visits

  • Communicate effectively with investigators, coordinators, physicians, and site staff

  • Verify investigator qualifications, facilities, equipment, and study resources

  • Review medical records and source documentation against CRFs

  • Ensure compliance with study protocols, SOPs, GCP guidelines, and regulatory requirements

  • Verify patient eligibility and enrollment criteria

  • Review and maintain regulatory documentation

  • Manage investigational product/device accountability and inventory

  • Review adverse events (AEs), serious adverse events (SAEs), and concomitant medications

  • Assess patient recruitment and retention performance

  • Prepare monitoring reports and follow-up documentation

  • Identify protocol deviations and recommend corrective actions


Eligibility Criteria

Required Qualifications

  • Bachelor's degree in Life Sciences, Health Sciences, Pharmacy, Biotechnology, Nursing, or a related field

  • 2–4 years of Clinical Research Associate (CRA) experience

  • Proficiency in Microsoft Office applications

  • Strong communication and presentation skills

  • Willingness to travel approximately 60–80% across India


Additional Benefits

  • Home-based work option available for CRAs with more than 1 year of monitoring experience

  • Structured career progression and promotion pathway

  • Exposure to multiple therapeutic areas and global clinical studies

  • Mentorship and leadership development opportunities

  • Competitive travel allowances and bonuses

  • Flexible work environment

  • Paid Time Off (PTO)

  • Employee wellness initiatives


About Medpace

Medpace is a global Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 professionals across 40+ countries and supports research in oncology, cardiology, endocrinology, CNS disorders, metabolic diseases, and infectious diseases.


Awards & Recognition

  • Forbes America's Most Successful Midsize Companies (2021–2024)

  • Multiple CRO Leadership Awards recognizing expertise, quality, reliability, and customer satisfaction