Senior Clinical Data Manager

Precision For Medicine

. Manage all aspects of clinical trial data management from study start-up through post-database lock for assigned projects .

Posted 10/27/2026full-timeRemote • Mexico, Brazil, ColombiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial data management, including oversight of data entry processes, database builds, and quality control. Proficient in managing timelines and resources while ensuring compliance with data management practices and standards.

Highest-signal resume keywords

Clinical Trial Data ManagementDatabase Build UATCRF Specifications DevelopmentMedical Coding (MedDRA, WHODrug)CDISC Standards Understanding

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ManagementClinical Database Management SystemsSAS ProgrammingQuality ControlData ReviewEdit Checks SpecificationTrial Master File ManagementMetrics ReportingResource ManagementTimeline Assessment

Soft Skills

Organizational SkillsCommunication SkillsLeadership SkillsInterpersonal SkillsProblem-Solving Skills

Tools & Technologies

Microsoft OfficeEDC VendorsClinical Trial Management Software

Industry Keywords

Clinical ResearchDrug DevelopmentBiologic DevelopmentOncology ExperienceOrphan Drug Therapeutic Experience

About the role

Key responsibilities & impact

Manage all aspects of clinical trial data management 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 data entry processes, including guidelines, training, quality, resourcing, and quality control
Assess and manage timelines, deadlines, and resource needs
Develop CRF specifications from clinical study protocols and coordinate stakeholder review
Assist with clinical database builds and conduct database build UAT
Maintain quality-controlled database build and data management documentation, including Trial Master File completeness
Specify and oversee edit checks and manual data review specifications
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 deliverables
Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input
Participate in SOP/process documentation development and maintenance
Communicate with study sponsors, vendors, and project teams regarding data and database issues
Provide leadership for cross-functional and organization-wide initiatives
Participate in meetings, presentations, proposals, project estimates, software demonstrations, and trainings
May assist with SAS programming and quality control of SAS programs
May require some travel
Perform other duties as assigned

Requirements

What you’ll need

Bachelor’s degree and/or a combination of related experience
8+ years’ experience for a Senior Clinical Data Manager; 10+ years for a Principal Clinical Data Manager
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Ability to handle a variety of clinical research tasks
Excellent organizational and communication skills
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, leadership, and interpersonal skills
Ability to undertake occasional travel
Preferred: experience in a clinical, scientific, or healthcare discipline
Preferred: dictionary medical coding (MedDRA and WHODrug)
Preferred: understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)
Preferred: oncology and/or orphan drug therapeutic experience
Candidates 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
Remote work arrangement
Some travel may be required