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Kite Pharma

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The Senior Data Management Associate will also work with Clinical Operations, Safety, and Regulatory as necessary. In this role you follow data management processes and understand the downstream ...

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Clinical Data Management Germany information

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How much do clinical data management germany jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for clinical data management germany in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Data Management professional in Germany, and why are they important?

To thrive as a Clinical Data Management professional in Germany, you need a strong understanding of clinical research processes, data management principles, and regulatory guidelines, often supported by a degree in life sciences or related fields. Familiarity with clinical data management systems (CDMS) like Medidata RAVE, EDC tools, and standards such as CDISC is typically required, and certifications like CCDM can be advantageous. Attention to detail, problem-solving ability, and effective communication are vital soft skills for ensuring data quality and collaborating across multidisciplinary teams. These competencies are crucial for maintaining compliance, ensuring data integrity, and supporting successful clinical trials.

What are some common challenges faced by Clinical Data Management professionals in Germany, and how can they be addressed?

Clinical Data Management professionals in Germany often navigate challenges related to strict data privacy regulations (such as GDPR), the integration of new digital health technologies, and ensuring data quality across multinational studies. Effective communication with cross-functional teams and staying updated on local regulatory changes are essential for success. Many organizations provide continuous training and support, which helps data managers adapt to evolving standards and collaborate efficiently with clinical, regulatory, and IT teams.

What is Clinical Data Management in Germany?

Clinical Data Management (CDM) in Germany refers to the process of collecting, cleaning, and managing clinical trial data to ensure its accuracy, reliability, and compliance with regulatory standards. Professionals in this field work with data from pharmaceutical or medical device studies, ensuring that all information is properly recorded and stored for analysis and reporting. CDM plays a critical role in the approval of new treatments by maintaining data integrity and protecting patient confidentiality, following both local (German) and international regulations such as GCP and GDPR.

What is the difference between Clinical Data Management Germany vs Clinical Data Coordinator Germany?

AspectClinical Data Management GermanyClinical Data Coordinator Germany
ResponsibilitiesDesigning, validating, and managing clinical data systems and databasesOverseeing data collection, entry, and quality control in clinical trials
Required SkillsData management, database software, regulatory knowledgeData entry, quality assurance, communication skills
Work EnvironmentPharmaceutical companies, CROs, clinical research settingsClinical trial sites, research organizations, CROs

Clinical Data Management Germany focuses on designing and maintaining clinical data systems, while Clinical Data Coordinator Germany handles data collection and quality at trial sites. Both roles require knowledge of clinical data processes but differ in scope and responsibilities.

Infographic showing various Clinical Data Management Germany job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 74% Full Time, 20% Part Time, and 3% Temporary. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.
Senior Manager, Clinical Data Management

Senior Manager, Clinical Data Management

Stratacuity: Proven Scientific Placement

Watertown, MA

Other

Posted 13 days ago

Job description

Our Watertown based client is seeking a Senior Manager, Clinical Data Management to lead end‑to‑end clinical data management activities across our development programs. In this role, you will ensure high‑quality, reliable clinical data from study startup through database lock while providing strategic and operational leadership. You will collaborate closely with cross‑functional teams, oversee CROs and external vendors, and contribute to process optimization and inspection readiness as our organization continues to grow.

Key Responsibilities

  • Lead and oversee data management activities for assigned clinical trials from study startup through database lock.
  • Partner with CROs and vendors to develop and review Data Management Plans, CRF Completion Guidelines, CRF design, database/edit check specifications, data review plans, data transfer specifications, and database lock deliverables.
  • Oversee EDC systems and ensure data integrity, consistency, and quality throughout the clinical trial lifecycle.
  • Manage external data management vendors and CRO partners, including performance oversight, issue escalation, quality expectations, timelines, and budget considerations.
  • Lead data review and cleaning activities, including query management, reconciliation, external data integration, and risk identification.
  • Collaborate with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Medical Monitoring, Safety, and Regulatory teams to resolve data‑related issues and support study deliverables.
  • Drive data management strategy to ensure alignment with clinical development goals and program timelines.
  • Develop, maintain, and enhance SOPs, templates, guidance documents, and best practices for clinical data management.
  • Identify operational risks and implement mitigation strategies to ensure inspection readiness and compliance with GCP, ICH, and regulatory requirements.
  • Support process improvement initiatives and contribute to building scalable, efficient data management operations.
  • Mentor junior team members and help strengthen data management capabilities across the organization.

Required Qualifications

  • Bachelor’s degree in a scientific, healthcare, or related field.
  • 8+ years of clinical data management experience in the pharmaceutical or biotechnology industry.
  • Proven experience independently leading data management activities across multiple clinical trials and/or programs.
  • Oncology clinical development experience strongly preferred.
  • Strong understanding of clinical trial processes, clinical data standards, GCP, ICH guidelines, and regulatory expectations.
  • Hands‑on experience with EDC systems, clinical databases, and related clinical technologies.
  • Experience managing CROs and external vendors, including oversight of deliverables, timelines, and quality.

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