Precision for Medicine

ClinicalDataManagerII/SeniorClinicalDataManager

$93–168k United States Remote Friendly
The Brief

“Clinical Data Manager II/Senior Clinical Data Manager at Precision for Medicine. Skills: Clinical data management, Database management, Data quality control. Manage clinical trial data management process. Oversee database development and testing”

What You'll Achieve.

Ensure deadlines are met with quality

Industry & Context.

Problems you'll solve

Troubleshoot operational problems; Identify issues; Identify obstacles; Identify barriers

Eligibility Requirements

Occasional travel

What They're Looking For.

Must Have

Bachelors and/or related experience, 8+ years Sr. Clinical Data Manager, 5 years Clinical Data Manager II, Proficiency in Microsoft Office, Handle clinical research tasks, Organizational and communication skills, Professional English (written and oral), Utilize clinical database systems, Broad knowledge of drug/device/biologic development, Effective data management practices, Representational skills, Communicate effectively orally and in writing, Leadership and interpersonal skills, Undertake occasional travel

Nice to Have

Experience in clinical, scientific or healthcare discipline, Dictionary medical coding (MedDRA and WHODrug), Understanding of CDISC standards, Oncology and/or Orphan Drug therapeutic experience

What You'll Do.

Manage clinical trial data management process

Oversee database development and testing

Serve as Primary Data Management contact

Ensure task continuity and responsiveness

Support Lead DM as back-up

Oversee project data entry process

Develop data entry guidelines

Manage data entry quality

Assess resource needs for projects

Develop CRF specifications

Coordinate CRF review/feedback

Assist in building clinical databases

Conduct database build UAT

Maintain quality controlled database build documentation

Oversee clinical database quality

Specify edit check requirements

Oversee edit check specification development

Oversee manual data review specification development

and maintain data management documentation

Oversee data management documentation completeness

Train clinical research personnel

Review and query clinical trial data

Perform line listing data review

Run patient and study level status reporting

Perform medical coding of medical terms

Ensure medical logic and consistency

Coordinate SAE/AE reconciliation

Liaise with third-party vendors

Support vendor timelines and data deliverables

Assist in reviewing protocols

Assist in reviewing SAP

Assist in reviewing CSR

Participate in SOP development

Participate in process documentation maintenance

Attend strategy meetings

Attend bid defense prep meetings

Attend capability presentations

Attend potential client engagement meetings

Review Request for Proposals (RFP)

Provide project estimates

Provide leadership for initiatives

Train data management project team members

Communicate with study sponsors

Communicate with vendors

Communicate with project teams

Present software demonstrations/trainings

Present department/company training sessions

Present at project meetings

Perform other duties as assigned

How You'll Work.

Team & Collaboration

Cross-functional initiatives; Project team members; Study sponsors; Vendors; Project teams

Communication Scope

Oral communication; Written communication; Presentations

Process & Methodology

Project management, Timeline management, Resource needs assessment

Free ATS check

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