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Principal Clinical Data Manager - US/Europe - Remote
Remote / Online - Candidates ideally in
Cary, Wake County, North Carolina, 27518, USA
Listed on 2026-06-24
Cary, Wake County, North Carolina, 27518, USA
Listing for:
Worldwide Clinical Trials Holdings, Inc.
Remote/Work from Home
position Listed on 2026-06-24
Job specializations:
-
IT/Tech
Data Analyst, Data Science Manager, Data Security
Job Description & How to Apply Below
This role is within Worldwide Clinical Trials’ Data Management team, which supports clinical studies from database design to final dataset delivery, ensuring data accuracy and integrity for regulatory submissions.
What you will do- Oversee, lead, manage and provide technical expertise within assigned complex projects/programs to ensure efficient, accurate and timely execution to the sponsor’s satisfaction.
- Provide subject matter expert support, solution management and departmental support for project initiatives and training.
- Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs.
- Liaise with DM Management at regular intervals to discuss progress and any outstanding issues (e.g., during Project Review Meetings).
- Collaborate with internal WCT departments working on the same project.
- Provide mentorship to other members of the DM department.
- Participate in and co-lead departmental initiatives for process improvement and efficiencies as defined by DM Departmental leadership.
- Deputise for Manager, DM as required.
- Support Business Development staff by participating in preparation of proposals and presentations to sponsors.
- Participate as necessary in sponsor audits, regulatory authority inspections and other third‑party meetings.
- Excellent attention to detail.
- Excellent written and verbal communication skills.
- Expert knowledge of data management best practices & technologies as applied to clinical trials.
- Excellent communication and interpersonal skills to collaborate with cross‑functional internal and external teams.
- Advanced understanding of clinical trial processes and protocol documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
- Strong independent analytical and problem‑solving skills.
- Independent and autonomous project oversight skills.
Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience.
Minimum of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
Compensation- The salary range for this position is annually:
United States of America - $99,000.00 - $. - 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.
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