Lead Clinical Data Manager II

Precision for Medicine; Oregon; Hybrid; USD 111,000 - 166,000; Full time

Benefits offered by this job

Discretionary annual bonus

Health insurance

Retirement savings benefits

Life insurance

Disability benefits

Parental leave

Paid time off

Job summary

Precision Medicine Group is seeking a Clinical Data Manager II to oversee all aspects of clinical trial data management from startup through database lock. You will lead data management activities, develop CRF specifications, coordinate with stakeholders, and ensure timely quality deliverables across studies.

The role requires 5+ years of CDM experience, proficiency with EDC and data management systems, and the ability to travel as needed.

Qualifications

• Bachelor's degree or equivalent combination of experience.
• 5+ years' Clinical Data Management experience.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Strong organizational and communication skills; fluent in English.
• Experience with a clinical database management system.
• Ability to undertake occasional travel.

Responsibilities

• Act as Lead DM and primary DM contact for assigned trials, ensuring continuity and timely delivery.
• Develop CRF specifications from study protocol and coordinate stakeholder feedback.
• Perform data entry, data quality checks, and review of trial data per Data Management Plan.
• Oversee database builds, UAT, and documentation for Trial Master File.
• Coordinate SAE/AE reconciliation and data queries with sponsors and vendors.
• May assist with SAS programming and QA of SAS programs in DM.

Skills

CDM experience

Microsoft Office

Documentation

Communication skills

Data management systems

Travel willingness

Education

Bachelor's degree or related experience

Tools

EDC software

SAS basics

Job description

Precision Medicine Group is seeking a Clinical Data Manager II to oversee all aspects of clinical trial data management from startup through database lock. You will lead data management activities, develop CRF specifications, coordinate with stakeholders, and ensure timely quality deliverables across studies.

The role requires 5+ years of CDM experience, proficiency with EDC and data management systems, and the ability to travel as needed.