Freelance (Senior) Clinical Data Manager

Progressive; München; Vor Ort; EUR 96.432 - 123.984; Vollzeit

Zusammenfassung

A leading biotech company in Munich is looking for a Freelance Senior Clinical Data Manager to ensure high data quality and regulatory compliance for clinical trials. You will lead data management activities, oversee CROs, and develop strategies aligned with data protection standards. The ideal candidate has a degree in Life Sciences, 4-8 years of experience in clinical data management and EDC systems, and strong communication skills in English. This opportunity offers a 12-month contract with the possibility of extension.

Qualifikationen

• Senior-level experience (4-8 years) in clinical data management.
• Strong expertise in EDC systems and collaboration with CROs.
• Fluency in English required; German not necessary.

Aufgaben

• Lead data management activities for clinical trials.
• Oversee and coordinate CROs and external vendors.
• Develop and execute data management strategies.

Kenntnisse

Clinical data management

EDC systems

SQL

SAS

R

Data visualization

Communication skills

Ausbildung

Degree in Life Sciences or related field

Jobbeschreibung

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. In this role, you will ensure high data quality, regulatory compliance, and efficient collaboration with internal teams and external vendors.

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?

Please submit your application directly via the platform.

SThree_Germany is acting as an Employment Business in relation to this vacancy.