Related skills
data reconciliation data management plan ecrf medidata rave oracle inform📋 Description
- Lead DM activities for clinical trials: DB setup, conduct, close-out.
- Collaborate cross-functionally to meet timelines and quality.
- Review protocols and CRFs; create/review eCRF specs.
- Develop DM docs: DMP, DVP, eCRF guidelines, data entry.
- Develop edit rules, checks, and query messages; perform UAT.
- Train sites; perform data review, reconciliation, metrics.
🎯 Requirements
- Bachelor's degree in clinical/pharmacy/biological sciences or nursing.
- At least 3 years data management experience in pharma.
- Knowledge of clinical research processes; GCP & ICH.
- Experience with Medidata Rave, Oracle InForm, OpenClinica, Medrio.
- Lead data management and ensure timelines/quality.
- MS Office (Outlook, Word, Excel, PowerPoint).
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