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

4-6 years
Not Disclosed
10 Nov. 4, 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

Position Title: Senior Clinical Research (CRA) Manager
Location: Navi Mumbai, India
Department: Clinical Monitoring
Job ID: 11494
Employment Type: Full-Time (On-site)
Organization: Medpace


Job Summary

Medpace, a leading full-service Clinical Research Organization (CRO), is expanding its Clinical Operations team. We are seeking an experienced Senior Clinical Research (CRA) Manager to lead and oversee our CRA team in Navi Mumbai. This role is crucial to the success of our clinical trial management process and offers a dynamic opportunity to grow within a global organization.


Key Responsibilities

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

  • Oversee CRA recruitment, training, onboarding, and ongoing professional development.

  • Ensure CRAs meet performance expectations related to core monitoring activities.

  • Manage CRA workload, resource allocation, and project assignments.

  • Monitor turnover and retention, implementing strategies to achieve company objectives.

  • Support operational excellence through process improvement and compliance adherence.


Qualifications

  • Bachelor’s degree in a life science or related discipline.

  • 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).

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

  • Strong leadership, mentoring, and motivational capabilities.

  • Excellent written and verbal communication skills.

  • Proficient in Microsoft Office Suite.

  • Willingness to travel occasionally (approximately 10%) for CRA evaluations.


About Medpace

Medpace is a scientifically driven global CRO providing Phase I–IV clinical development services for biotechnology, pharmaceutical, and medical device companies.

  • Headquarters: Cincinnati, Ohio

  • Global Presence: 40+ countries

  • Employees: 5,000+ professionals

Medpace specializes in multiple therapeutic areas including oncology, cardiology, endocrinology, metabolic disorders, infectious diseases, and CNS research.


Why Join Medpace?

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

Perks & Benefits

  • Flexible work environment

  • Competitive compensation and benefits

  • Generous PTO and structured career growth paths

  • Company-sponsored events and wellness initiatives

  • Recognition as one of America’s Most Successful Midsize Companies (Forbes, 2021–2024)

  • Recipient of multiple CRO Leadership Awards from Life Science Leader magazine


Next Steps

Qualified candidates will be contacted by a Medpace recruiter with details regarding the interview process.

#CRO2024 | #ClinicalResearch | #MedpaceCareers