Senior Clinical Data Manager

Worldwide Clinical TrialsDurham, North Carolinaonsite$79k–$157kView the original posting at Worldwide Clinical Trials ↗

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials , we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Senior Clinical Data Manager at Worldwide Take ownership of clinical data management across multiple complex, global projects and programs, leading activities from study start-up through conduct and closeout. You’ll apply your technical expertise and independent judgment to help ensure high-quality data is delivered accurately, efficiently, and on time. In this senior role, you’ll partner with sponsors and cross-functional teams while overseeing data cleaning, database lock activities, resources, budgets, timelines, and project risks. You’ll also have the opportunity to strengthen data management practices by leading process reviews and sharing your expertise through training, support, and mentorship. Where You'll Work This is a remote role open to candidates based in US. You will collaborate with global teams across multiple time zones. What You'll Do Lead end-to-end data management activities across multiple complex global projects and programs, from start-up through database lock and closeout. Develop key data management documentation, including Data Management Plans, database specifications, edit check specifications, CCGs, and Data Transfer Agreements. Oversee UAT, data cleaning, external vendor reconciliation specifications, and database lock activities to support accurate and timely study delivery. Allocate resources and monitor project scope, budgets, timelines, risks, and performance metrics, escalating concerns when appropriate. Represent Data Management in internal, sponsor, and study meetings, providing technical expertise and clear input on project progress and issues. Collaborate with cross-functional teams and Data Management leadership to resolve challenges and keep study activities moving forward. Lead and contribute to process reviews and improvements that strengthen data management practices. Train, support, and mentor other Data Management team members, sharing expertise and best practices. Participate in sponsor audits, regulatory authority inspections, and other third-party meetings as needed. What You'll Bring Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience, plus a minimum of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. Strong knowledge of clinical data management best practices and technologies used in clinical trials. Strong understanding of clinical trial processes and key study documents, including protocols, statistical analysis plans, CRFs, and study reports. Proven ability to independently oversee projects, manage priorities, and solve complex problems with excellent attention to detail. Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external cross-functional teams. Proficiency in English. Discover the Difference We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers , or connect with us on LinkedIn . At Worldwide Clinical Trials

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