Senior Clinical Data Manager

Worldwide; Durham (NC); Remoto; USD 79.000 - 157.000; Tempo pieno

Descrizione del lavoro

Worldwide Clinical Trials seeks a Senior Clinical Data Manager to take ownership of data management across multiple global projects from study start-up through database lock. This senior role requires independent judgment and strong CDM expertise to ensure high-quality data delivered on time.

You will collaborate with sponsors and cross-functional teams, develop data management documentation, oversee data cleaning and UAT, and help advance data management practices while guiding junior staff in

Competenze

• Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or related field; 5+ years clinical data management experience.
• Strong knowledge of clinical data management best practices and trial processes.
• Ability to oversee projects independently with attention to detail.
• Excellent communication and collaboration with cross-functional teams.

Mansioni

• Lead end-to-end data management across multiple global projects from start-up through database lock.
• Develop data management documents like 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 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 input on 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.

Conoscenze

Data management

Leadership

Communication

English proficiency

Formazione

Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or related discipline

Descrizione del lavoro

Senior Clinical Data Manager page is loaded## Senior Clinical Data Managerremote type: Remotelocations: Durham, North Carolinatime type: Full timeposted on: Posted Todayjob requisition id: JR103034Join 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 WorldwideTake 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 WorkThis 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, or connect with us on .At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):United States of America - $79,000.00 - $157,000.00The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law**.**