Senior Associate, Clinical Research

MSD; Gurugram District; On-site; INR 600,000 - 1,200,000; Full time

Job summary

MSD is seeking a Senior Associate in Clinical Research in India to manage trial and site administration, ensuring adherence to clinical guidelines and robust document control. The role collaborates with multiple stakeholders to drive successful trial execution.

Responsibilities include tracking essential documents, updating trial databases, coordinating supply management, and supporting regulatory submissions and site start-up tasks.

Qualifications

• Bachelor’s degree in Life Sciences or related field
• Experience in clinical research or trial management
• Familiarity with regulatory guidelines and compliance

Responsibilities

• Manage trial and site administration activities
• Track essential documents and report safety findings
• Update clinical trial databases and trackers
• Coordinate clinical supply management with country roles
• Prepare and archive clinical documents, including eTMF
• Support regulatory submissions and site start-up processes

Skills

Trial management

Documentation management

Regulatory compliance

Clinical research knowledge

Education

Bachelor's degree in Life Sciences

Tools

eTMF system

Clinical trial databases

Job description

The Senior Associate in Clinical Research will be responsible for managing trial and site administration, ensuring compliance with clinical guidelines, and overseeing document management. This role requires collaboration with various stakeholders to ensure the successful execution of clinical trials.

Responsibilities

• Manage trial and site administration activities
• Track essential documents and report safety findings
• Update clinical trial databases and trackers
• Coordinate clinical supply management with country roles
• Prepare and archive clinical documents, including eTMF
• Support regulatory submissions and site start-up processes

Qualifications

• Bachelor's degree in Life Sciences or related field
• Experience in clinical research or trial management
• Familiarity with regulatory guidelines and compliance