Senior Clinical Data Manager

Precision Medicine Group

. Manage all aspects of the clinical trial data management process from study start-up 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

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Demonstrates extensive experience in clinical trial data management, including database build, quality control, and compliance with data management plans. Proficient in leading cross-functional teams and communicating effectively with stakeholders in the clinical research environment.

Highest-signal resume keywords

Clinical Data ManagementDatabase Build UATSAS ProgrammingOncology ExperienceMicrosoft Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management ProcessCRF Specifications DevelopmentMedical CodingData Quality OversightStatistical Analysis Plans ReviewTrial Master File ManagementDatabase MigrationOperational Problem SolvingLine-Listing Data ReviewQuality Control of SAS Programs

Soft Skills

LeadershipOrganizational SkillsCommunication SkillsInterpersonal SkillsRepresentational Skills

Tools & Technologies

Clinical Database Management SystemsEDC VendorsMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Outlook

Industry Keywords

Clinical Research OrganisationPharmaceuticalBiotechDrug DevelopmentDevice DevelopmentBiologic Development

About the role

Key responsibilities & impact

Manage all aspects of the clinical trial data management process from study start-up through post-database lock for assigned projects
Serve as primary Data Management contact and Lead Data Manager 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 and feedback
Conduct database build UAT and maintain controlled database-build documentation
Oversee clinical database quality and edit-check specifications
Create, revise, version, and maintain data-management documentation and Trial Master File completeness
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 third-party data and EDC vendors regarding timelines and data deliverables
Assist with SAS programming and quality control of SAS programs
Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input
Review and provide feedback on protocols, Statistical Analysis Plans, and Clinical Study Reports as required
Participate in developing and maintaining SOPs and process documentation
Participate in strategy meetings, bid-defense preparation, capability presentations, and client-engagement meetings
Review RFPs, proposals, and project estimates
Provide leadership for cross-functional and organization-wide initiatives
Communicate with sponsors, vendors, and project teams regarding data and database issues
Present software demonstrations, trainings, and project meetings
Perform other duties as assigned; occasional travel may be required

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
Set up and database migrations experience
Oncology experience preferred
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Professional use of the English language, written and oral
Experience utilizing 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

Regular full-time employment
Equal Opportunity Employer
Reasonable accommodation available for applicants with disabilities
No employer sponsorship required; candidates must be legally authorized to work in the country of employment