Senior Clinical Data Manager: Lead DM, Data Quality & Systems

Precision Medicine Group

United States

Remote

USD 190,000 - 285,000

Full time

9 days ago
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Benefits offered by this job

Bonus potential
Private medical insurance
MultiSport Card
Life insurance
Pension
Home working allowance
Vacation

Job summary

Precision Medicine Group is seeking a Clinical Data Manager II/Senior Clinical Data Manager to manage the full data lifecycle of assigned clinical trials, from startup through post database lock. You will lead data management efforts, develop CRFs, coordinate with sponsors and vendors, and ensure timely, high-quality data delivery.

The role requires 8+ years in data management or 5+ years as CDM II in CRO/biotech, oncology experience preferred, and strong MS Office skills.

Qualifications

  • 8+ years’ experience as a Sr. Clinical Data Manager or 5+ Years as a Clinical Data Manager II working for a CRO/pharma/biotech company.
  • Experience setting up data management and database migration
  • Oncology experience preferred
  • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
  • Experience with various clinical database management systems and overall data management best practices

Responsibilities

  • Lead DM role for assigned projects/programs with back-up continuity.
  • Oversee data entry processes, guidelines, QA and resourcing.
  • Develop CRF specifications from the protocol and coordinate stakeholder feedback.
  • Conduct database build UAT and maintain build documentation.
  • Coordinate SAE/AE reconciliation and data queries; liaise with vendors as needed.

Skills

Data management leadership
Communication skills
Travel ability
Regulatory knowledge (SOP/WI)

Education

Bachelor's degree

Tools

Microsoft Word
Microsoft Excel
PowerPoint
Outlook
SAS programming

Job description

Precision Medicine Group is seeking a Clinical Data Manager II/Senior Clinical Data Manager to manage the full data lifecycle of assigned clinical trials, from startup through post database lock. You will lead data management efforts, develop CRFs, coordinate with sponsors and vendors, and ensure timely, high-quality data delivery.

The role requires 8+ years in data management or 5+ years as CDM II in CRO/biotech, oncology experience preferred, and strong MS Office skills.

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