Program Clinical Data Manager

## Program Clinical Data Manager Apply:
Remote:
Durham, North Carolina:
Full time:
Posted Today:
JR103035

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  Take ownership of clinical data management across complex, global projects and programs, helping ensure high-quality data is delivered accurately, efficiently, and on time.

In this senior role, you’ll lead data management activities from study start-up through database lock and close-out, partnering with sponsors and cross-functional teams throughout the clinical trial lifecycle.  You’ll also bring your expertise beyond individual studies, serving as a subject matter expert, mentoring colleagues, strengthening data management processes, and contributing to departmental initiatives. Your leadership will help teams address risks, maintain quality, and deliver work that meets sponsor expectations.  

## 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
* * data management activities independently across multiple complex global projects and programs, from study start-up through conduct, database lock, and close-out.
* ** Plan
* * resources, timelines, budgets, scope, and risks to keep data management deliverables on track and escalate concerns appropriately.
* ** Develop and oversee
** key trial documentation, including Data Management Plans, database and edit check specifications, completion guidelines, data transfer agreements, and vendor reconciliation specifications.
* ** Drive
* * effective user acceptance testing, data cleaning, reconciliation, metrics reporting, and database lock activities to support accurate and timely clinical data.
* ** Partner
* * with sponsors and internal cross-functional teams, representing Data Management in study meetings and contributing technical expertise and solutions.
* ** Serve
* * as a subject matter expert for assigned data management processes, providing guidance and training while maintaining relevant process and guidance documentation.
* ** Lead
* * responses to process-related quality issues, including root cause analysis and corrective and preventive actions as required.
* ** Mentor
* * Data Management colleagues and contribute to departmental initiatives focused on improving processes, quality, and efficiency.
* ** Support
* * business development proposals and sponsor presentations, and participate as needed in 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, plus a minimum of 7 years of clinical data management or related experience 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…