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

5+ years
Not Disclosed
10 Sept. 16, 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
Functional Area: Clinical Monitoring
Job ID: 11494
Employment Type: Full-time
Work Arrangement: Office-based


Job Summary:

Medpace is seeking a Senior Clinical Research (CRA) Manager to join the Clinical Monitoring team in Navi Mumbai. This role plays a key part in managing clinical trial monitoring activities, providing leadership, mentoring, and operational oversight of Clinical Research Associates (CRAs).

This position is ideal for candidates looking to leverage their clinical monitoring expertise while developing further in a management role.


Key Responsibilities:

  • Line Management: Supervise and mentor Clinical Research Associates (CRAs).

  • Recruitment & Training: Manage recruitment, onboarding, and ongoing development of CRAs.

  • Oversight & Performance: Ensure CRAs meet expectations regarding core monitoring responsibilities.

  • Resource Management: Track and manage CRA assignments, allocation, and workload.

  • Retention: Manage CRA turnover and retention to meet organizational objectives.

  • Occasional Travel: Evaluate CRAs in-person (approximately 10%).


Qualifications:

  • Education: Bachelor’s degree in a relevant field.

  • Experience:

    • 4–6 years pharmaceutical industry experience in clinical monitoring or study management.

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

  • Skills & Knowledge:

    • Advanced knowledge of Good Clinical Practice (GCP).

    • Strong leadership, mentoring, and motivational skills.

    • Effective written and verbal communication skills.

    • Proficient in Microsoft Office (Word, Excel, PowerPoint).


Medpace Overview:

Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services for biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace:

  • Flexible work environment.

  • Competitive compensation and benefits package.

  • Paid time off and structured career growth opportunities.

  • Company-sponsored employee appreciation events.

  • Employee health and wellness initiatives.

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).

  • Multiple CRO Leadership Awards from Life Science Leader magazine.