Senior Clinical Data Manager

Worldwide Clinical Trials

. Lead end-to-end data management activities across multiple complex global projects and programs, from start-up through database lock and closeout .

Posted 11/2/2026full-timeRemote • North Carolina • United StatesSenior💰 $79,000 - $157,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, including the development of Data Management Plans and oversight of data cleaning and reconciliation processes. Proven ability to lead cross-functional teams, manage project timelines and budgets, and ensure compliance with regulatory standards.

Highest-signal resume keywords

Clinical Data ManagementData Management PlansProject OversightRegulatory ComplianceCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management PlansDatabase SpecificationsEdit Check SpecificationsUATData CleaningVendor ReconciliationClinical Trial ProcessesStatistical Analysis PlansCRFsStudy Reports

Soft Skills

Excellent CommunicationInterpersonal SkillsProblem SolvingAttention to DetailMentoring

Industry Keywords

Biomedical SciencesLife SciencesPharmaceutical IndustryBiotechnologyMedical Device Industry

About the role

Key responsibilities & impact

Lead end-to-end data management activities across multiple complex global projects and programs, from start-up through database lock and closeout
Develop 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
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
Collaborate with cross-functional teams and Data Management leadership to resolve challenges
Lead and contribute to process reviews and improvements
Train, support, and mentor Data Management team members
Participate in sponsor audits, regulatory authority inspections, and other third-party meetings as needed

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 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

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Equal employment opportunities
Opportunities to learn, grow, and shape the future of clinical research
Training, support, and mentorship opportunities