Das ist der Job
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Darum lohnt es sich
In this role, you will ensure high data quality, regulatory compliance, and efficient collaboration with internal teams and external vendors.
Overview
Project Opportunity: Senior Clinical Data Manager (m/f/x)
Start: ASAP
Location: on-site in Munich
Duration: 12 month / extendable
We are seeking an experienced Freelance (Senior) Clinical Data Manager to support a leading biotech company in managing and overseeing clinical study data.
Responsibilities
• Lead data management activities for clinical trials in close collaboration with Clinical Operations
• Oversee and coordinate CROs and external vendors
• Develop and execute data management strategies aligned with CDISC, GCP, FDA/EMA guidelines
• Prepare and maintain essential documentation (DMPs, DVPs, DTAs)
• Ensure data integrity and smooth data workflows across all study phases
• Guarantee compliance with GDPR, HIPAA, and other data protection standards
• Support regulatory submissions with high-quality datasets and documentation
Your Profile
• Degree in Life Sciences or a related field; senior-level experience (4-8 years)
• Strong expertise in clinical data management and EDC systems
• Proven experience collaborating with CROs
• Bonus: SQL, SAS, R, or data visualization experience
• Excellent communication skills with fluency in English (German not required)
• Reliable, structured, quality-driven work approach
Interested?
SThree_Germany is acting as an Employment Business in relation to this vacancy.
