Related skills
sas edc clinical data management quality control sops📋 Description
- Lead DM for assigned projects; ensure back-up and timely tasks.
- Oversee data entry with guidelines, training, quality, and resourcing.
- May perform QC of data entry and ensure data accuracy.
- Manage timelines and resources; ensure DM deadlines are met.
- Develop CRF specifications from protocol; coordinate stakeholder feedback.
- Conduct database build UAT and maintain QA documentation.
🎯 Requirements
- Bachelor's degree or related experience.
- 8+ years as Sr. CDM or 5+ years as CDM II in CRO/Pharma/Biotech.
- Oncology experience preferred.
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
- Strong leadership, organization, and communication; occasional travel.
- Experience with clinical DB systems; SAS programming exposure.
🎁 Benefits
- Discretionary annual bonus
- Private medical insurance
- MultiSport Card
- Life insurance
- Pension
- Home working allowance
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