PrecisionMedicineGroup

Manage all aspects of clinical trial data management from study start up to post database lock
Primary Data Management contact (Lead DM role) for assigned projects; support other Lead DMs as
Oversee project data entry process, develop data entry guidelines, training, quality and resourcing
Perform quality control of data entry when needed
Provide input, assess and manage timelines; ensure deadlines are met with quality
Develop CRF specifications from clinical study protocol and coordinate review/feedback from

🎯 Requirements

Bachelors or combination of related experience
10+ years experience
Microsoft Office: Word, Excel, PowerPoint, Outlook
Ability to handle a variety of clinical research tasks
Excellent organizational and communication skills
Professional use of English; both written and oral

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