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Associate Director Clinical Data Management Jobs in Renton, WA

Director, Clinical Data Management

Redmond, WA ยท 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 ...

Manager, Clinical Data Management

Seattle, WA ยท Remote

CA$99K - CA$166K/yr

Oversee development of direct reports by setting and tracking individual objectives and key results ... Ensure Data Management deliverables for projects assigned meet/exceed project/study team ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management ... Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management ... Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in ...

Clinical Data Analyst, Spotfire

Redmond, WA ยท On-site

$90K - $130K/yr

The Spotfire Clinical Data Analyst will specialize in the installation, maintenance, and ... Manage and continually improve the Spotfire analytics environment, ensuring data integrity ...

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Associate Director Clinical Data Management information

See Renton, WA salary details

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How much do associate director clinical data management jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for associate director clinical data management in Renton, WA is $43.99, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $43.99 per hour, depending on experience, location, and employer.

What are Associate Director Clinical Data Management?

An Associate Director of Clinical Data Management is a senior professional responsible for overseeing the planning, execution, and management of data collected in clinical trials within the pharmaceutical or biotechnology industry. They ensure that all clinical data is accurate, secure, and compliant with regulatory standards. This role typically involves leading teams, developing data management strategies, collaborating with cross-functional departments, and ensuring that projects are delivered on time and within budget. Associate Directors also play a key role in establishing best practices and continuous process improvements within the data management function.

What are the key skills and qualifications needed to thrive as an Associate Director Clinical Data Management, and why are they important?

To thrive as an Associate Director Clinical Data Management, you need a strong background in clinical research, data management, and regulatory compliance, typically supported by a life sciences degree and several years of experience in clinical data management. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and industry standards such as CDISC or GCP is crucial, with certifications like CCDM being advantageous. Leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and ensure accurate data delivery. These competencies are vital because they ensure high-quality, compliant data management that supports successful clinical trials and regulatory submissions.

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

AspectAssociate Director Clinical Data ManagementClinical Data Manager
ResponsibilitiesOversees data management teams, develops strategies, ensures data quality and complianceManages data collection, validation, and database setup for clinical trials
Required CredentialsBachelor's/Master's in life sciences, experience in data management, leadership skillsBachelor's in life sciences, experience in clinical data handling, technical skills
Work EnvironmentSenior-level, strategic, often in larger organizations or departmentsOperational, hands-on, often in CROs or pharmaceutical companies

The Associate Director Clinical Data Management typically holds a higher strategic role, overseeing teams and ensuring data quality across projects, while the Clinical Data Manager focuses on day-to-day data handling tasks. Both roles require similar educational backgrounds and technical skills, but differ in scope and level of responsibility.

What are some common challenges faced by an Associate Director of Clinical Data Management, and how can they be addressed?

Associate Directors in Clinical Data Management often encounter challenges such as maintaining data quality across multiple studies, managing tight timelines, and ensuring compliance with evolving regulatory requirements. To address these, they implement robust data review processes, foster close collaboration between cross-functional teams (like biostatistics, clinical operations, and IT), and promote continuous training for their teams. Strong leadership and effective communication are key to navigating these challenges while delivering high-quality data for clinical trials.
What job categories do people searching Associate Director Clinical Data Management jobs in Renton, WA look for? The top searched job categories for Associate Director Clinical Data Management jobs in Renton, WA are:
What cities near Renton, WA are hiring for Associate Director Clinical Data Management jobs? Cities near Renton, WA with the most Associate Director Clinical Data Management job openings:
Infographic showing various Associate Director Clinical Data Management job openings in Renton, WA as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $91,134 per year, or $43.8 per hour.
Director, Clinical Data Management

Director, Clinical Data Management

SystImmune, Inc

Redmond, WA โ€ข On-site

$190K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 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.