This position as a Clinical Trial Associate at Takeda in Gurgaon, Haryana, may be ideal for you if you’re looking for a career in clinical research with a reputable, international pharmaceutical firm. The Global Portfolio Division of Takeda is offering the opportunity to participate in state-of-the-art research and development through this post.
Takeda is a global biopharmaceutical company that is values-driven, R&D-focused, and dedicated to improving people’s health and prospects all across the world. Takeda, with its rich history and dedication to innovation, is focused on creating medications that can change patients’ lives and help create a fair and sustainable healthcare system.
Responsibilities in the Job
You will be in charge of managing the Electronic Trial Master File (eTMF) and Clinical Trial Management Systems (CTMS) on a daily basis as a Clinical Trial Associate at Takeda. Among your main duties are:
- overseeing the creation of eTMF plans tailored to each study.
- checking the documents that have been submitted to the eTMF for quality.
- ensuring that the documentation for clinical trials complies with regulatory regulations, ICH-GCP guidelines, and eTMF specifications.
- tracking and recognizing eTMF patterns unique to a research and responding to eTMF system inquiries.
- helping with tasks connected to audits and inspections.
- assisting the manager or lead of clinical operations in carrying out CRO oversight.
- working together with research teams to set up programs, venues, and investigations in CTMS.
- organizing meetings to set standards, escalate problems, and guarantee that CTMS features work as intended.
Qualifications and Skills
In order to succeed in this position, you ought to have:
- a bachelor’s degree in science or a closely linked field in healthcare, at the very least.
- three or more years of expertise in clinical research and TMF that is appropriate, ideally in a pharmaceutical, biotechnology, or CRO setting.
- It is strongly desirable if you have experience with Veeva Vault CTMS & eTMF, or any eTMF system software.
- a thorough knowledge of local clinical trial laws and GCP.
- strong problem-solving, communication, and organizing abilities.
- a track record of consistent success throughout the previous two to three years.
How to Apply
Apply for the Takeda, Gurgaon Clinical Trial Associate job by going to the Takeda careers portal and looking for Job ID R0120735 under the Research & Development section. To start the application process, click the “Apply” button. Make sure the information you provide is correct and current. Join Takeda and help create a better future by supporting cutting-edge clinical research.
