
Job description
Oversee, lead, manage, and provide technical expertise within assigned projects to ensure efficient, accurate, and timely execution to the Sponsor's satisfaction. Provide fully independent and autonomous leadership of data management services across multiple complex global projects/programs.
Prepare DM trial documentation, ensure effective UAT, write external vendor reconciliation specifications, oversee data cleaning activities, produce metrics to monitor progress, and represent Worldwide DM at internal and external study meeting calls.
Excellent attention to detail, excellent written and verbal communication skills, strong knowledge of data management best practices & technologies, and strong analytical and problem-solving skills are required.
Company

Healthcare
Worldwide Clinical Trials is a global contract research organization that partners with biopharmaceutical companies to manage clinical development from early‑stage, first‑in‑human studies through Phase III registration trials. With more than 4,400 professionals operating in over 70 countries, the firm provides therapeutic expertise in neuroscience, oncology, rare diseases, immunology, cardiovascular/metabolic disorders, and cell and gene therapies. The company offers a flexible service model that includes full‑service trial management and functional service partnerships (Worldwide Flex), emphasizing a people‑first, collaborative approach that enhances data transparency and decision‑making. Its capabilities span protocol development, regulatory support, trial optimization, pharmacovigilance, bioanalysis, and on‑site pharmacy, delivering tailored solutions that meet the evolving demands of clinical research.
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