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Senior Clinical Research (Cra) Manager - Based In Navi Mumbai, India

4-6 years
Not Disclosed
10 Oct. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research (CRA) Manager

📍 Location: Navi Mumbai, India
🏢 Department: Clinical Monitoring
🆔 Job ID: 11494


Job Summary

Medpace’s Clinical Operations team is expanding rapidly, and we are seeking a full-time, office-based Senior Clinical Research (CRA) Manager to join our Clinical Monitoring team in Navi Mumbai, India.

This position plays a key leadership role in managing and guiding CRAs (Clinical Research Associates) to ensure the successful conduct of clinical trials. If you are an experienced professional looking to advance your career in clinical research management, this opportunity is for you.


Key Responsibilities

  • Lead and manage a team of Clinical Research Associates (CRAs).

  • Oversee CRA recruitment, training, and continuous professional development.

  • Monitor CRA performance to ensure high-quality site monitoring and adherence to company standards.

  • Manage and track CRA resource allocation and workload distribution.

  • Implement strategies to reduce turnover and improve CRA retention.

  • Conduct periodic CRA evaluations (approx. 10% travel).


Qualifications

  • Education: Bachelor’s degree in Life Sciences or a related field.

  • Experience:

    • 4–6 years of experience in the pharmaceutical or CRO industry (clinical monitoring or study management).

    • Minimum 3 years as a CRA and 1–2 years in a CRA Manager role preferred.

  • Technical Skills:

    • Advanced understanding of Good Clinical Practice (GCP) guidelines.

    • Proficient in Microsoft Office applications.

  • Soft Skills:

    • Strong leadership, mentoring, and motivational abilities.

    • Excellent written and verbal communication skills.


About Medpace

Medpace is a full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.

With headquarters in Cincinnati, Ohio, Medpace operates in 40+ countries and employs 5,000+ professionals worldwide. The company’s mission is to accelerate global development of safe and effective medical therapeutics through scientific and disciplined processes.

Therapeutic Expertise Includes:
Oncology • Cardiology • Metabolic Disease • Endocrinology • CNS • Anti-Viral • Anti-Infective


Why Join Medpace?

People. Purpose. Passion. Make a Difference Tomorrow — Join Us Today.

  • Flexible work environment

  • Competitive salary and benefits package

  • Attractive PTO (Paid Time Off) plans

  • Structured career growth and development programs

  • Employee appreciation and recognition events

  • Health and wellness initiatives


Awards & Recognition

🏆 Forbes: America’s Most Successful Midsize Companies (2021–2024)
🏆 Life Science Leader: CRO Leadership Awards for Expertise, Quality, Capabilities, Reliability, and Compatibility


What to Expect Next

A Medpace representative will review your application.
If shortlisted, you will be contacted with details for the next steps.

Apply Now
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