Clinical Data Manager

Worldwide Clinical Trials

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

Posted 11/2/2026full-timeRemote • North Carolina • United StatesSeniorLead💰 $99,000 - $196,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical data management, including the development of Data Management Plans and oversight of database activities. Proven ability to lead cross-functional teams, mentor colleagues, and ensure compliance with clinical trial processes and quality standards.

Highest-signal resume keywords

Clinical Data ManagementData Management PlansUser Acceptance TestingRegulatory ComplianceLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data Management Best PracticesDatabase Lock ActivitiesData CleaningMetrics ReportingRoot Cause AnalysisStatistical Analysis PlansCompletion GuidelinesData Transfer AgreementsVendor Reconciliation SpecificationsStudy Reports

Soft Skills

Analytical SkillsProblem-Solving SkillsAttention to DetailCommunication SkillsInterpersonal Skills

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryMedical Device IndustryClinical TrialsStudy Start-UpStudy ConductDatabase ManagementSponsor AuditsQuality IssuesProcess Documentation

About the role

Key responsibilities & impact

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, and escalate concerns appropriately
Develop and oversee Data Management Plans, database and edit check specifications, completion guidelines, data transfer agreements, and vendor reconciliation specifications
Drive user acceptance testing, data cleaning, reconciliation, metrics reporting, and database lock activities
Partner with sponsors and internal cross-functional teams and represent Data Management in study meetings
Serve as a subject matter expert, providing guidance and training and maintaining process documentation
Lead responses to process-related quality issues, including root cause analysis and corrective and preventive actions
Mentor Data Management colleagues and contribute to departmental process, quality, and efficiency initiatives
Support business development proposals and sponsor presentations
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 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 the clinical trial process and key documents, including protocols, statistical analysis plans, CRFs, and study reports
Strong independent leadership, analytical, and problem-solving skills
Excellent attention to detail
Excellent communication and interpersonal skills
Proficiency in English, with strong written and verbal communication skills

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Equal employment opportunities
Transparent compensation and pay equity