Lead Clinical Data Manager — Trial Data Excellence

Precision Medicine Group (New York, United States); United States; Remote; USD 101,000 - 166,000; Full time

Benefits offered by this job

Discretionary annual bonus

Health insurance

Retirement savings plan

Life insurance

Disability benefits

Parental leave

Paid time off

Job summary

Precision Medicine Group in the United States is seeking an experienced Clinical Data Manager II to lead data management activities from study startup to database lock. You will develop CRF specifications, oversee database builds, perform UAT, and ensure timely, high-quality data deliverables across assigned trials.

The role requires 5+ years in clinical data management, strong MS Office skills, and experience with clinical DBMS and CDISC standards. Some travel may be required.

Qualifications

• Bachelor's degree or a combination of related experience
• 5+ years of Clinical Data Management experience
• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
• Fluent English communication
• Experience with a clinical DBMS and knowledge of CDISC standards preferred
• Ability to travel as needed

Responsibilities

• Serve as Primary Data Management contact (Lead DM) for assigned projects
• Perform data entry and QA of data for paper-CRF studies as needed
• Develop CRF specifications from study protocol and coordinate stakeholder feedback
• Oversee database build, UAT, and data management documentation
• Train CRAs, site staff and other personnel on study-specific items
• Coordinate SAE/AE reconciliation and data query resolution
• Generate line listings, study metrics, and data reporting
• Liaise with third-party vendors and potentially support SAS programming
• Contribute to SOPs and process documentation

Skills

Clinical Data Management

MS Office

Communication skills

English fluency

Travel flexibility

Education

Bachelor's degree

Tools

Clinical DBMS

Job description

Precision Medicine Group in the United States is seeking an experienced Clinical Data Manager II to lead data management activities from study startup to database lock. You will develop CRF specifications, oversee database builds, perform UAT, and ensure timely, high-quality data deliverables across assigned trials.

The role requires 5+ years in clinical data management, strong MS Office skills, and experience with clinical DBMS and CDISC standards. Some travel may be required.