Clinical Trial Manager

MUMBAI (IN)ONSITEPOSTED: 7/23/2026
PHARMAFull-time
HIRING ORGANIZATIONMEDPACE, INC.Clinical Research / Pharmaceutical Services
Medpace, Inc.

ROLE DEFINITION & RESPONSIBILITIES

EXTERNAL AGGREGATED LISTING

This is a quick-info listing fetched from our external partner portals. Detailed candidate qualifications and descriptions are available on the official application page.

Manages overall clinical trial deliverables and vendor coordination, ensures strict compliance with ICH-GCP protocols, oversees trial timelines, and coordinates cross-functional global teams.

REQUIRED VERIFIED SKILLS

Clinical Trial Management
ICH-GCP
Project Management
Clinical Operations

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Mid-to-senior management CRO compensation packages in India reflect multi-region trial oversight responsibilities.

ORGANIZATION CONTEXT & CULTURE

Medpace, Inc. is a global full-service clinical research organization (CRO) that provides scientifically-driven clinical development services to the pharmaceutical, biotechnology, and medical device industries. They specialize in conducting Phase I-IV clinical trials across various therapeutic areas, leveraging deep therapeutic expertise to accelerate the development and approval of new drugs and devices. Medpace aims to bring new and effective medical products to patients faster.

TEAM SIZE: 5,001-10,000 employees
INDUSTRY: Clinical Research / Pharmaceutical Services

EXPECTED CAREER ROADMAP

Direct ladder toward Senior CTM, Project Director, or Portfolio Management within global trial operations.

APPLICATION ADVISORY

Highlight prior experience leading global or Phase I-IV trials, site management, and protocol compliance.
RECOMMENDED TRAINING
1/5

READY TO SUBMIT?

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