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Director Clinical Data Management Jobs (NOW HIRING)

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

SystImmune is seeking an experienced and strategic Director, Clinical Data Management to lead the clinical data management function across our portfolio. This individual will be responsible for ...

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Director Clinical Data Management information

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$244K

How much do director clinical data management jobs pay per year?

As of Aug 4, 2026, the average yearly pay for director clinical data management in the United States is $154,873.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,000.00 and $189,500.00 per year, depending on experience, location, and employer.

What are typical challenges faced by a director clinical data management, and how can a candidate prepare for them?

As a Director of Clinical Data Management, you may encounter challenges such as managing cross-functional teams, ensuring data integrity across complex global trials, and staying current with changing regulatory guidelines. Effective directors address these challenges through strong project management, robust communication, and fostering a culture of continuous process improvement. Candidates can prepare by gaining hands-on experience with major data management systems, keeping up with industry best practices, and developing leadership abilities to motivate diverse teams. Proactively identifying and resolving potential data issues is also key to success in this strategic role.

What is a director clinical data management?

A Director of Clinical Data Management oversees the collection, processing, and quality control of clinical trial data to ensure accuracy, compliance, and regulatory adherence. They manage data management teams, develop protocols, and implement data standards to support clinical research. This role requires expertise in regulatory guidelines (e.g., FDA, ICH-GCP), database systems, and statistical processes. The director collaborates with cross-functional teams, including biostatisticians, clinical operations, and regulatory affairs, to ensure data integrity throughout the trial lifecycle.

What are the key skills and qualifications needed to thrive as a director clinical data management?

To thrive as a Director Clinical Data Management, you need extensive experience in clinical data management, good knowledge of regulatory requirements, and usually an advanced degree in a related field. Familiarity with clinical trial data systems like EDC (Electronic Data Capture), CDISC standards, and certifications such as CCDM (Certified Clinical Data Manager) are commonly expected. Outstanding leadership, problem-solving, and communication skills help you manage teams and collaborate across departments. These competencies are crucial for ensuring high-quality, compliant data that supports successful clinical trials and regulatory submissions.

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Director Clinical Data Management jobs near you
Infographic showing various Director Clinical Data Management job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $154,873 per year, or $74.5 per hour.

Director, Clinical Data Management

Revolution Medicines

Redwood City, CA • Hybrid

Other

Posted 17 days ago

Job description

The Opportunity:

This position has a key role in the day-to-day management of Clinical Data Management (CDM) activities. Including timely and professional management of clinical trial data for all relevant phases. Represents Revolution Medicines (RevMed) CDM in Clinical Team meetings. The Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management strategy. Identifies requirements for capturing and processing of clinical data ensuring accuracy, consistency, and completeness. Manage external vendors providing clinical data. Manages and/or perform data management tasks according to strict quality standards including SAE reconciliation, third party vendor data reconciliation, medical coding processing, protocol deviation collection, query management to identify errors and inconsistencies in clinical data and ensure their resolution. Provides CDM oversight of outsourced and partner-resourced clinical trials including scoping trials, project management, relationship management, approval of deliverables, and coordination of internal reviewers.

  • Plans, coordinates, and manages CDM tasks for clinical studies.

  • Participate and review CRO proposals.

  • Acts as primary liaison with CROs, third party data vendors, EDC vendors.

  • Reviews clinical protocols and cross functional plans.

  • Serves as primary reviewer or author of case report forms (CRFs) and CRF completion guidelines.

  • Overseas and participates in all aspects of EDC database development, testing, maintenance, and lock/unlock.

  • Ensures Data Management Plans are followed through the course of the studies.

  • Sets and manages Data Management project timelines.

  • Provides comprehensive status updates to project team members.

  • Address data issues identified by cross-functional team members, accountable for external data vendor documentation, management, and reconciliation.

  • Assist in defining and creating data listings, summary table validation, data specifications, and process data transfers in preparation for statistical review and data management audit.

  • Implements data standardization and maintains data model across projects.

  • Direct management and mentoring responsibilities for internal data management team members.

  • Lead department initiatives e.g., development of SOPs.

  • Other duties as assigned.

Required Skills, Experience and Education: 

  • MS, BS/BA degree, or other suitable qualification with relevance to the field.

  • 15 or more years' direct experience of designing and running early-stage or late-stage clinical trials.

  • Knowledge of, and experience with, clinical databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures.

  • Good working knowledge of ICH, FDA, and GCP regulations and guidelines.

  • A demonstrable record of strong leadership and teamwork.

  • Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.

  • Excellent written and verbal communication skills.

  • Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important.

  • Experience from industry is essential.

Preferred Skills:

  • Oncology experience, especially in solid tumors.

  • 5 or more years' direct line management experience. 

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