Related skills
sas cdisc sdtm veeva adam📋 Description
- Lead DM for assigned projects, ensuring timely tasks and continuity.
- Oversee data entry, guidelines, training, and data quality.
- Develop CRF specs and coordinate stakeholder feedback.
- Build and maintain clinical databases; perform UAT & documentation QA.
- Coordinate SAE/AE reconciliation and vendor communications.
- Train staff on CRF/EDC; support protocol/SAP reviews; travel may be required.
🎯 Requirements
- Bachelor’s degree and/or related experience.
- 8+ years of clinical data management experience.
- Excellent organizational and communication skills.
- Experience with Medidata Rave and Veeva systems.
- Knowledge of CDISC standards (CDASH, SDTM, ADaM).
- Oncology and/or Orphan Drug experience; MedDRA/WHODrug coding.
- Strong leadership and collaboration; travel ability.
🎁 Benefits
- Professional development and cross-functional leadership.
- Training sessions and skill growth opportunities.
- Exposure to global trial operations and data mgmt.
- Inclusive, equal-opportunity employer culture.
- Travel may be required for some roles.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Data Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!