Clinical Data Manager II

Precision Medicine Group

. Manage all aspects of the clinical trial data management process from study start-up to post-database lock for assigned projects under some supervision .

Posted 11/4/2026full-timeRemote • United StatesMid-LevelSenior💰 $100,700 - $166,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Data Management, including database build, quality control, and data review processes. Proficient in managing clinical trial data from start-up to post-database lock while ensuring compliance with industry standards and effective communication with stakeholders.

Highest-signal resume keywords

Clinical Data ManagementDatabase Build Quality ControlSAS ProgrammingMedical CodingCDISC Standards

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data EntryQuality ControlCRF Specifications DevelopmentData Management DocumentationClinical Database Management SystemOncology Therapeutic ExperienceMedDRA CodingWHODrug CodingStatistical Analysis System (SAS)Metrics Reporting

Soft Skills

Organizational SkillsCommunication SkillsTraining SkillsProblem-Solving SkillsTeam Collaboration

Tools & Technologies

Microsoft OfficeElectronic Data Capture (EDC)Trial Master FileClinical Research ToolsData Management Software

Industry Keywords

Clinical TrialsDrug DevelopmentBiologic DevelopmentData Management PracticesStandard Operating Procedures (SOPs)

About the role

Key responsibilities & impact

Manage all aspects of the clinical trial data management process from study start-up to post-database lock for assigned projects under some supervision
Serve as primary Data Management contact and/or contributor for assigned clinical projects/programs
Perform data entry for paper-CRF studies and quality control of data entry as needed
Provide input into timelines and ensure clinical data management deadlines are met with quality
Assess resource needs for assigned projects as needed
Develop CRF specifications from clinical study protocols and coordinate stakeholder review and feedback
Assist in building clinical databases
Conduct database build UAT and maintain quality-controlled database build documentation
Oversee overall clinical database quality
Specify requirements for electronic, manual data review, and other edit checks
Create, revise, version, and maintain data management documentation and oversee Trial Master File completeness
Train clinical research personnel and data management project team members on study-specific CRFs, EDC, and related items
Review and query clinical trial data according to the Data Management Plan
Perform line-listing data review
Run patient- and study-level status and metric reporting
Perform medical coding of medical terms
Coordinate SAE/AE reconciliation
Liaise with third-party data and EDC vendors in a project manager capacity
Assist with SAS programming and quality control of SAS programs
Identify and troubleshoot operational problems using metrics data, audit reports, and stakeholder input
Review and provide feedback on protocols, SAPs, and CSRs as required
Participate in developing and maintaining SOPs and process documentation
Attend strategy meetings, bid-defense preparation, capability presentations, and client engagement meetings as needed
Review RFPs, proposals, and provide project estimates
Communicate with sponsors, vendors, and project teams regarding data, database, and project issues
Present software demonstrations, trainings, and project meetings
Perform other duties as assigned

Requirements

What you’ll need

Bachelor's degree and/or a combination of related experience
5+ years’ Clinical Data Management experience or demonstrated aptitude in the key skills for the role
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Able to handle a variety of clinical research tasks
Excellent organizational and communication skills
Must be able to read, write, speak fluently and comprehend the English language to enable communication across Precision for Medicine and with clients
Experience in utilizing a clinical database management system
Broad knowledge of drug, device and/or biologic development and effective data management practices
Ability to undertake occasional travel
Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Preferred: Understanding of dictionary medical coding (MedDRA and WHODrug)
Preferred: Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)
Preferred: Oncology therapeutic experience

Benefits

Comp & perks

Discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation
Equal opportunity employment
Reasonable accommodation during the application process