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Executive Director Clinical Data Management Jobs

SystImmune, Inc

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Xencor, Inc.

Director, Clinical Data Management

San Diego, CA · On-site

$195 - $240/hr

  • Medical

  • Retirement

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 ...

Eisai

Executive Director, Clinical Data Science

... clinical trial efficiency and accelerate innovation. The Executive Director will spearhead the ... Manage and mentor a diverse team of data scientists and people managers across geographies.

Socket.dev

Director, Clinical Data Management

Bedford, MA · On-site

$225 - $244/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Director of Clinical Data Management will be responsible for leading data management activities for one or more development programs and serves as the highest point of escalation within Data ...

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Executive Director Clinical Data Management information

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$51.5K

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

As of Aug 17, 2026, the average yearly pay for executive director clinical data management in the United States is $100,124.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $109,000.00 per year, depending on experience, location, and employer.

What is an executive director clinical data management?

An Executive Director of Clinical Data Management is a senior leader responsible for overseeing the collection, validation, and management of clinical trial data within a pharmaceutical or biotechnology company. They develop and implement strategies to ensure data accuracy, regulatory compliance, and the successful delivery of clinical trial results. This role involves managing teams, collaborating with cross-functional departments, and ensuring that data management processes support the company's research and development goals. Executive Directors also stay updated on industry best practices and regulatory requirements to continuously improve data management systems.

How does an executive director clinical data management typically collaborate with other departments in a pharmaceutical or clinical research organization?

An Executive Director of Clinical Data Management works closely with cross-functional teams, including clinical operations, biostatistics, regulatory affairs, and IT departments. They facilitate data flow by setting standards for data collection, ensuring compliance, and leading discussions to resolve data-related issues. Effective collaboration is essential to align timelines, support regulatory submissions, and maintain data integrity throughout the clinical trial process. Strong communication and leadership skills are critical, as the role often involves guiding teams and influencing strategic decisions across the organization.

What are the key skills and qualifications needed to thrive as an executive director clinical data management, and why are they important?

To excel as an Executive Director Clinical Data Management, you typically need advanced knowledge of clinical research, data management principles, and regulatory guidelines, supported by a relevant degree and extensive industry experience. Mastery of clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with standards such as CDISC is expected, along with certifications like CCDM being advantageous. Outstanding leadership, strategic decision-making, and effective communication skills help drive teams and ensure alignment across departments. These competencies are crucial for ensuring high-quality, compliant clinical data that supports successful drug development and regulatory submissions.

What is the difference between Executive Director Clinical Data Management vs Clinical Data Manager?

AspectExecutive Director Clinical Data ManagementClinical Data Manager
ResponsibilitiesOversees entire clinical data management operations, strategic planning, and team leadershipManages data collection, validation, and database setup for specific clinical trials
Required CredentialsTypically advanced degrees (e.g., MS, PhD), extensive experience, leadership skillsBachelor’s or Master’s degree in life sciences, experience in data management
Work EnvironmentSenior management in pharmaceutical or biotech companies, overseeing multiple projectsClinical research sites, CROs, or pharmaceutical companies, focused on trial-specific tasks

The Executive Director Clinical Data Management holds a strategic leadership role overseeing data management across projects, while the Clinical Data Manager focuses on executing data collection and validation tasks within specific trials. Both roles require relevant experience, but the executive position involves broader oversight and decision-making responsibilities.

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Executive Director Clinical Data Management jobs near you
Infographic showing various Executive Director Clinical Data Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $100,124 per year, or $48.1 per hour.

Director, Clinical Data Management

SystImmune, Inc

Redmond, WA • On-site

$190K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
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 overseeing all aspects of clinical data management activities from study start-up through database lock and regulatory submission. The Director will provide leadership for internal and external data management teams, ensure high-quality and inspection-ready clinical data, and contribute to the development and execution of data management strategies supporting global clinical trials.
The successful candidate will collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Pharmacovigilance, Regulatory Affairs, and external partners to ensure timely and compliant delivery of clinical data for decision-making and regulatory submissions.
This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations.
Responsibilities
  • Lead and oversee the Clinical Data Management function, including strategy, standards, processes, and operational execution across the development portfolio.
  • Build and scale a high-performing data management infrastructure to support a growing clinical pipeline.
  • Serve as a key cross-functional leader in clinical development planning and execution.
  • Oversee all data management activities for Phase I-III clinical trials from study start-up through database lock and regulatory submission.
  • Ensure the delivery of high-quality, complete, and reliable clinical data through effective data review, issue management, and quality oversight.
  • Drive timely database lock and submission-ready data deliverables in accordance with study timelines.
  • Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory requirements, while maintaining inspection readiness.
  • Establish and maintain CDISC-compliant data standards and industry best practices to support regulatory submissions.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, and Safety teams to support study execution, data review, and submission readiness.

Qualifications
  • Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field required; Master's degree preferred.
  • Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
  • At least 5 years of leadership experience managing data management teams, vendors, and CRO partnerships.
  • Significant experience supporting oncology clinical trials across early- and late-stage development.
  • Demonstrated experience supporting regulatory submissions (NDA, BLA, MAA) and health authority inspections.
  • Expertise with EDC systems, external data integrations, data reconciliation, and database management.
  • Strong knowledge of clinical trial databases, CDISC standards, coding dictionaries (e.g., MedDRA, WHO Drug), and clinical data workflows.
  • Familiarity with risk-based quality management principles, GCP requirements, and clinical development processes.
  • Working knowledge of biostatistics, statistical analysis, and clinical data reporting to support cross-functional collaboration.
  • Proven leadership, strategic thinking, problem-solving, communication, and stakeholder management skills, with a track record of driving cross-functional collaboration and operational excellence in a fast-paced biotech environment.

Preferred Qualifications
  • Oncology and/or antibody-drug conjugate (ADC) development experience.
  • Experience managing global clinical trials across multiple regions.
  • Prior experience in a growing biotechnology company.

Compensation and Benefits:
The expected base salary range for this position is $190,000 - $250,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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