Senior Clinical Data Manager

Precision For Medicine

. Manage all aspects of the clinical trial data management process from study startup through post-database lock for assigned projects .

Posted 9/29/2026full-timeRemote • United Kingdom, Poland, Hungary, Romania, Serbia, SlovakiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in clinical trial data management, including database setup, quality control, and compliance with regulatory standards. Proficient in leading cross-functional teams and communicating effectively with stakeholders in the clinical research environment.

Highest-signal resume keywords

Clinical Trial Data ManagementDatabase Setup and MigrationsOncology ExperienceSAS ProgrammingClinical Database Management Systems

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management DocumentationCRF Specifications DevelopmentMedical CodingQuality Control of SAS ProgramsData Review and QueryingTrial Master File DocumentationEdit-Check SpecificationsLine-Listing Data ReviewUAT Database BuildResource Management

Soft Skills

LeadershipOrganizational SkillsCommunication SkillsInterpersonal SkillsRepresentational Skills

Tools & Technologies

Microsoft OfficeEDC VendorsClinical Database Management Systems

Industry Keywords

Clinical Research OrganisationPharmaceuticalBiotechDrug DevelopmentDevice DevelopmentBiologic DevelopmentSOPsWIsRegulatory DirectivesData Management Plan

About the role

Key responsibilities & impact

Manage all aspects of the clinical trial data management process from study startup through post-database lock for assigned projects
Follow SOPs/WIs, regulatory directives, study-specific plans, and guidelines
Serve as primary Data Management contact or Lead DM for assigned clinical projects/programs
Oversee project data entry, including guidelines, training, quality, and resourcing
Assess and manage timelines, deadlines, and resource needs
Develop CRF specifications and coordinate stakeholder review when required
Conduct database build UAT and maintain controlled database documentation
Oversee clinical database quality and edit-check specifications
Create, revise, version, and maintain data management documentation and Trial Master File documentation
Train clinical research personnel and data management project team members
Review and query clinical trial data according to the Data Management Plan
Perform line-listing data review and patient/study-level status and metric reporting
Perform medical coding and coordinate SAE/AE reconciliation
Liaise with external data and EDC vendors regarding timelines and data-related deliverables
Assist with SAS programming and quality control of SAS programs when needed
Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input
Review and provide feedback on protocols, SAPs, and CSRs when required
Participate in SOP and process documentation development and maintenance
Support strategy meetings, bid defenses, capability presentations, client engagement meetings, RFP reviews, proposals, and project estimates
Provide leadership for cross-functional and organization-wide initiatives
Communicate with sponsors, vendors, and project teams regarding project issues
Present software demonstrations, trainings, and project meetings
Perform other assigned duties

Requirements

What you’ll need

Bachelor's degree and/or a combination of related experience
8+ years’ experience as a Senior Clinical Data Manager or 5+ years as a Clinical Data Manager II working for a Clinical Research Organisation, Pharmaceutical or Biotech company
Experience with setup and database migrations
Oncology experience preferred
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Professional use of the English language, written and oral
Experience using various clinical database management systems
Broad knowledge of drug, device and/or biologic development and effective data management practices
Strong representational, organizational, communication, leadership, and interpersonal skills
Ability to undertake occasional travel
Must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Equal Opportunity Employer
Reasonable accommodation available for applicants with disabilities
Some travel may be required
AI-generated insights during the application journey with an opt-out option