Program Clinical Data Manager

Worldwide Clinical Trials

. Lead data management activities independently across multiple complex global projects and programs from study start-up through conduct and close-out .

Posted 11/4/2026full-timeRemote • North Carolina • United StatesSeniorLead💰 $99,000 - $196,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, overseeing complex global projects, and ensuring compliance with best practices in clinical trials. Proficient in developing Data Management Plans and managing cross-functional communication and training.

Highest-signal resume keywords

Clinical Data ManagementData Management PlansProject OversightRegulatory ComplianceCross-Functional Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessDatabase SpecificationsEdit Check SpecificationsData CleaningUATRoot Cause AnalysisCAPAsStatistical Analysis PlansCRFsStudy Reports

Soft Skills

Problem SolvingAttention to DetailMentoringInterpersonal CommunicationWritten Communication

Industry Keywords

Biomedical SciencesLife SciencesPharmaceutical IndustryBiotechnologyMedical Device Industry

About the role

Key responsibilities & impact

Lead data management activities independently across multiple complex global projects and programs from study start-up through conduct and close-out
Develop and oversee Data Management Plans, database specifications, edit check specifications, CCGs, and Data Transfer Agreements
Drive UAT, data cleaning, external vendor reconciliation, progress metrics, and timely database lock activities
Manage data management resources, timelines, scope, budgets, and risks; escalate concerns and keep leadership informed
Represent Data Management in internal and external study meetings with sponsors and cross-functional teams
Serve as a subject matter expert, 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 process, quality, and efficiency initiatives
Support sponsor proposals and presentations and contribute expertise during sponsor audits, regulatory inspections, and third-party meetings

Requirements

What you’ll need

Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a 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
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
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
Proficiency in English

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Equal employment opportunities
Opportunities to learn and grow
Mentoring and professional development through training