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Job description
We are seeking a detail-oriented and quality-focused Data Manager for Clinical Trials to join our team. The successful candidate will play a critical role in the clinical research project, working with large volumes of clinical or medical data.
Responsibilities will include tracking database set-up, testing, and maintenance, communicating with clients and project teams, reviewing study documents, and designing eCRF, Data Management, and Data Validation Plans.
If you have experience managing clinical or medical data, proficiency in Clinical Data Management systems, and strong organizational and time management skills, this could be a great opportunity for you.
Company
Healthcare
PSI CRO is a leading full-service global contract research organization that specializes in predictable patient enrollment and on-time project delivery across a broad therapeutic portfolio, including oncology, hematology, multiple sclerosis, infectious diseases, and radiopharmaceuticals. Leveraging rigorous feasibility assessments and a dedicated research team, PSI delivers accurate study timelines and high-quality data in more than 50 countries worldwide. The company’s no-nonsense, results-driven approach is reflected in its high client retention, referral rates, and low staff turnover. With a focus on Phase 2, Phase 3, and pivotal trials, PSI provides end-to-end clinical trial management, ensuring seamless execution from protocol design through regulatory submission.
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