Takeda Hiring Clinical Trial Associates

Takeda Hiring Clinical Trial Associates

At Takeda, Clinical Trial Associate Positions: Ensuring Quality and Compliance in Clinical Research Discover the exciting opportunity to work as a clinical trial associate at Takeda, a leading pharmaceutical and biotechnology company in the world. This post explores the duties, requirements, and essential elements of becoming a member of Takeda’s Clinical Operations team in Gurgaon, Haryana.

Clin Trial Associate Positions at Takeda in Gurgaon: Headline Steering Clinical Excellence

Understanding Takeda Pharmaceuticals

Takeda is committed to advancing healthcare through innovative research and development. As a Clinical Trial Associate, you’ll be part of Takeda’s Clinical Operations team, contributing to the management and oversight of clinical trial documentation and processes.

Objectives and Accountabilities of a Clinical Trial Associate

In this role, your key responsibilities include:

  • Managing CTMS (Clinical Trial Management System) and eTMF (electronic Trial Master File), ensuring compliance with regulations and Takeda’s standards.
  • Leading the development of study-specific eTMF plans.
  • Performing quality control of eTMF documents and addressing system-related queries.
  • Maintaining Essential Document Lists (EDLs) and identifying study-specific trends for communication to relevant teams.
  • Supporting inspection/audit activities and contributing to CRO oversight.
  • Collaborating with study team leads to set up studies and ensure CTMS functionality meets study requirements.
  • Leading meetings to address system issues, trends, and standards for continuous improvement.

Education, Behavioral Competencies, and Skills Required

To excel in this role, candidates should have:

  • A minimum Bachelor’s degree in a science/healthcare field.
  • 3+ years of relevant clinical research and TMF (Trial Master File) experience.
  • Previous experience with eTMF system software, preferably Veeva Vault CTMS & eTMF.
  • Strong knowledge of GCP (Good Clinical Practice) and local clinical trial regulations.
  • Organizational, problem-solving, communication, and negotiation skills.

How to Apply

Interested, eligible candidates should apply for Clinical Trial Associate Position. Click here 

Travel Requirements and Work Environment

The role may require domestic travel (20-30%) and limited international travel (10-20%), with some weekend commitments. As an employee of Takeda, you’ll work in a dynamic and collaborative environment, contributing to the advancement of healthcare solutions.

To apply for this job please visit jobs.takeda.com.

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