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.
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Takeda Hiring Clinical Trial Associates[/caption]
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.
https://pharmastuff.org.in/job/h0unbq6sjmzh7qlkaypymvqnjow21vfuwk1cbasz
