Program Clinical Data Manager

Worldwide Clinical TrialsDurham, North Carolinaonsite$99k–$196kView 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 Program Clinical Data Manager at Worldwide Bring your clinical data management expertise to complex global projects and programs where strong leadership, technical excellence, and reliable delivery matter. As a Program Clinical Data Manager, you’ll independently lead data management activities from study start-up through conduct and close-out, helping ensure high-quality delivery that meets sponsor expectations. You’ll provide oversight across timelines, resources, budgets, risks, data cleaning, vendor reconciliation, and database lock activities while partnering with cross-functional teams and sponsors. You’ll also serve as a subject matter expert, helping strengthen data management processes, training, and quality across the department. Beyond individual projects, you’ll have the opportunity to mentor colleagues, co-lead process improvement initiatives, support proposals and sponsor presentations, and contribute your expertise during audits and regulatory inspections. Where You'll Work This is a remote role open to candidates based in the US. You will collaborate with global teams across multiple time zones. What You'll Do Lead data management activities independently across multiple complex global projects and programs, from study start-up through conduct and close-out. Develop and oversee key trial documentation, including Data Management Plans, database specifications, edit check specifications, CCGs, and Data Transfer Agreements. Drive effective UAT, data cleaning, external vendor reconciliation, progress metrics, and timely database lock activities. Manage data management resources, timelines, scope, budgets, and risks, escalating concerns appropriately and keeping leadership informed of project progress. Represent Data Management in internal and external study meetings, collaborating with sponsors and cross-functional teams to support effective project delivery. Serve as a subject matter expert for assigned data management processes, providing guidance and training while driving quality issue resolution, root cause analysis, CAPAs, and guidance-document updates. Mentor Data Management colleagues and co-lead departmental initiatives that improve processes, quality, and efficiency. Support business development through sponsor proposals and presentations, and contribute data management expertise during sponsor audits, regulatory authority inspections, and other third-party meetings. What You'll Bring Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience, along with a minimum of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. Expert knowledge of clinical data management best practices and technologies as applied to clinical trials. Advanced understanding of the clinical trial process and key study documents, including protocols, statistical analysis plans, CRFs, and study reports. Demonstrated ability to independently oversee complex projects, solve problems, analyze issues, and maintain strong attention to detail. Excellent written, verbal, interpersonal, and cross-functional communication skills for w

The people who work here are one introduction away.

We show you who they are and write your first message — the insider list for this posting is filling in now. You have one introduction. The rest follows.

People at Worldwide Clinical Trials you can reach out to

29 of 58 public LinkedIn profiles found in searches for Worldwide Clinical Trials list Worldwide Clinical Trials in their headline — those are the ones you can be confident work there. Pick who to reach out to — we'll draft your message; you make the contact. The rest, when shown, are marked Unverified.

Profiles are public pages as indexed by the search engine — we never log in to LinkedIn or copy private data, and anyone can ask to be removed. Ask to be removed →

Start the conversation More Clinical data jobs