Neurocrine Biosciences in the United Kingdom is seeking a detail-oriented Clinical Trials Operations Professional to support planning, initiation, conduct and close-out of assigned clinical studies. You will work with CTMs, CROs and investigator sites to ensure trials conform to GCP, FDA/EU requirements and robust data integrity.
Key tasks include managing essential document collection, IRB/IEC submissions, study timelines, site monitoring support, and maintaining eTMF quality.
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Clinical Trials Specialist – Start-Up & IRB Support in London employer: Neurocrine Biosciences
Neurocrine Biosciences is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. With a strong commitment to employee growth, you will have access to ongoing training and development opportunities, ensuring your career progresses alongside the company's mission to improve patient lives. Located in a vibrant area, the company provides a supportive environment where your contributions directly impact global health outcomes.
