Freelance (Senior) Clinical Data Manager

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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?

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