Clinical Data Manager II: Lead DM & Database Build

Precision Medicine Group; United States; Remote; USD 101.000 - 166.000; Vollzeit

Benefits dieser Stelle

Discretionary annual bonus

Health insurance

Retirement savings benefits

Life insurance

Disability benefits

Parental leave

Paid time off for sick leave and VAC

Zusammenfassung

Precision Medicine Group is seeking a Clinical Data Manager II to oversee the clinical trial data management process from study start-up to post database lock. You will lead DM activities, develop CRF specifications, and ensure data quality and timely delivery in line with SOPs and regulatory directives.

The role includes coordinating with vendors, building databases, performing UAT, and training staff as needed to maintain data integrity across trials.

Qualifikationen

• 5+ years’ Clinical Data Management experience or demonstrated aptitude in key skills.
• Proficiency with Microsoft Office: Word, Excel, PowerPoint, Outlook.
• Ability to handle a variety of clinical research tasks and read/write/speak English fluently.
• Experience with clinical databases and data management best practices.

Aufgaben

• Serve as primary DM contact and lead DM on assigned projects.
• Develop CRF specifications from the study protocol and coordinate reviews.
• Oversee database build, UAT, and quality documentation.
• Query and review trial data according to the Data Management Plan.
• Coordinate with vendors and may assist SAS programming.
• Provide input into timelines and resource assessment; ensure deadlines.

Kenntnisse

Clinical Data Management

MS Office Proficiency

English Proficiency

Task prioritization

Communication skills

Ausbildung

Bachelor's degree or related experience

Tools

SAS programming

Clinical database management system

Microsoft Office Suite

Jobbeschreibung

Precision Medicine Group is seeking a Clinical Data Manager II to oversee the clinical trial data management process from study start-up to post database lock. You will lead DM activities, develop CRF specifications, and ensure data quality and timely delivery in line with SOPs and regulatory directives.

The role includes coordinating with vendors, building databases, performing UAT, and training staff as needed to maintain data integrity across trials.