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sas edc cdisc sdtm adam📋 Description
- Lead DM for assigned projects; ensure back-up, continuity, and timely tasks.
- Oversee data entry process, guidelines, training, quality, and resourcing.
- May perform data entry quality checks.
- Develop CRF specs from protocol and coordinate stakeholder feedback; may assist in building databases.
- Conduct database build UAT and maintain QA documentation; oversee database quality.
- Specify edit check requirements; oversee spec development and reviews.
🎯 Requirements
- 8+ years' experience as Senior Clinical Data Manager; 5 years as CDM II.
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
- Experience with various clinical database management systems.
- Broad knowledge of drug, device and/or biologic development and data management practices.
- Strong leadership and interpersonal skills; excellent written and verbal communication.
- Ability to travel occasionally.
🎁 Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance
- Disability benefits
- Paid time off for sick leave and vacation
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