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Xencor

Director, Clinical Data Management

San Diego, CA · On-site

We have an excellent opportunity for a Director, Clinical Data Management , to join our team. This position will be based out of our San Diego, CA. office and is a minimum 2 days a week onsite hybrid ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

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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 14, 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.
Manager, Clinical Data Management

Manager, Clinical Data Management

Crispr Therapeutics

South Boston, MA • On-site

$123K - $133K/yr

Full-time

Posted 8 days ago

Job description

Job Description:
Company Overview
Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom.
Position Summary
The Manager of Clinical Data Management will lead clinical data management activities in support of CRISPR studies across all stages of clinical development. They will ensure that clinical data capture, systems and processes will ensure accurate, consistent, high quality, and complete data.
The successful candidate will provide clinical data management oversight of outsourced clinical trials, including but not limited to: project management, vendor management, coordination of internal reviews, and approval of deliverables. The candidate will impact multiple clinical development programs, health authority submissions, presentations and publications across internal and external stakeholders.
Responsibilities
  • Plan, coordinate, and manage data management tasks and timelines.
  • Act as primary liaison with CROs, third party data vendors, and EDC vendors.
  • Collaborate with internal clinical study team to ensure all stakeholders' needs are addressed.
  • Primary author/approver for CRFs, CCGs, edit check specifications, SAE reconciliation plans, Coding plans, Data Management Plans, and third party vendor data specifications.
  • Oversee database design, production and UAT cycles, ensuring that the CRO meets the highest quality standards.
  • Accountable for external data vendor documentation, management, and reconciliation.
  • Contribute to departmental SOP and process development and improvement, and integration of technology.
  • Perform and/or review medical coding and SAE reconciliation.
  • Support internal review/QC of clinical data.
  • Support GCP inspection readiness.

Minimum Qualifications
  • Bachelor's degree in a health-related field is required, Master's degree strongly preferred
  • Minimum of 7+ years of progressive experience in clinical data management in a regulatory environment.
  • Demonstrated proficiency managing the lifecycle of clinical data projects.
  • Experience developing reports using J-Review, Business Objects, or other CDM reporting tools.
  • Experience with EDC databases, especially Medidata Rave.
  • Experience with CDASH/SDTM/CDISC standards.
  • Experience working with central and specialty labs/vendors.
  • Working knowledge of medical terminology and medical coding dictionaries including MedDRA and WHO.
  • Familiarity with GCP, ICH and FDA requirements as applicable for Clinical Data Management.
  • Ability to manage multiple initiatives and shifting priorities within a small, fast paced company environment.
  • Strong analytical and problem-solving skills that meet or improve the status quo.
  • Excellent interpersonal skills with the ability to work independently and collaboratively in a dynamic team environment.
  • Excellent written and oral communication skills.

Preferred Qualifications
  • Prior experience working in a small or medium-sized biotech or pharmaceutical company

Competencies
  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.

CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Manager: Base pay range of $123,000 to $133,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

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