Senior Clinical Data Manager - Lead Data Operations

Precision Medicine Group; Oregon; Hybrid; USD 134,000 - 201,000; 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 Senior Clinical Data Manager to oversee data management for clinical trials from start-up through database lock. You will develop CRF specifications, supervise data entry, QC, database builds, and ensure timely, high-quality deliverables.

Strong leadership and communication skills are essential. The role requires 8+ years of experience in data management, proficiency with clinical DBMS, and familiarity with CDISC standards.

Qualifications

• Bachelor's degree or equivalent in a related field.
• 8+ years' experience as a Clinical Data Manager.
• Proficiency with Microsoft Office applications.
• Experience with clinical database management systems.
• Strong written and verbal communication skills.

Responsibilities

• Act as Primary Data Management contact for assigned projects, ensuring continuity and timely task execution.
• Oversee data entry processes, develop guidelines, training, and data-entry quality.
• Quality control of data entry and overall data management documentation.
• Develop CRF specifications from study protocols and coordinate stakeholder feedback.
• Perform/ oversee SAS programming when needed, and QA of SAS outputs.
• Coordinate SAE/AE reconciliation and data query resolution.
• Prepare status reports and metrics on data management progress.

Skills

Data management leadership

Project coordination

Excellent communication

Organizational skills

English proficiency

Education

Bachelor's degree or equivalent in a related field

Tools

SAS programming

MS Office (Word/Excel/PowerPoint/Outlook)

EDC systems

Clinical database management systems

Job description

Precision Medicine Group is seeking a Senior Clinical Data Manager to oversee data management for clinical trials from start-up through database lock. You will develop CRF specifications, supervise data entry, QC, database builds, and ensure timely, high-quality deliverables.

Strong leadership and communication skills are essential. The role requires 8+ years of experience in data management, proficiency with clinical DBMS, and familiarity with CDISC standards.