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Contract Clinical Data Manager Jobs in Renton, WA

Fred Hutchinson Cancer Center

Data Engineer IV

Seattle, WA · On-site

$130K - $156K/yr

Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation ... Independently organize and manage multiple complex projects, priorities, and technical initiatives ...

Pfizer

Head of AI Clinical Excellence

Bothell, WA

$89K - $121K/yr

Partner with digital, data science, and technology teams to design, build, validate, and deploy AI ... Drive organizational adoption through education, change management, and capability building.

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Contract Clinical Data Manager information

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$22

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$92

How much do contract clinical data manager jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for contract clinical data manager in Renton, WA is $64.30, according to ZipRecruiter salary data. Most workers in this role earn between $50.82 and $76.54 per hour, depending on experience, location, and employer.

What does a contract clinical data manager do?

A Contract Clinical Data Manager typically spends their days overseeing data collection, validation, and entry processes, ensuring that clinical trial data meets quality and regulatory standards. This role often involves close collaboration with data entry teams, biostatisticians, and clinical project managers to resolve discrepancies and maintain data integrity. Daily responsibilities may include designing case report forms, conducting data reviews, managing database queries, and preparing data for interim or final analyses. Working on a contract basis, you may manage multiple projects concurrently and must be adaptable to varying timelines and sponsor requirements.

What is a contract clinical data manager?

A Contract Clinical Data Manager is a temporary or freelance professional responsible for overseeing and managing clinical trial data for pharmaceutical, biotech, or CRO companies. They ensure data integrity, compliance with regulatory standards, and support database design, data cleaning, and reporting. Contract roles offer flexibility and typically involve working on specific projects or trials for a set duration.

What are the key skills and qualifications needed to thrive as a contract clinical data manager?

To thrive as a Contract Clinical Data Manager, you need strong expertise in clinical data management, a background in life sciences, and familiarity with regulatory guidelines such as FDA or ICH-GCP. Proficiency in database systems like Medidata Rave or Oracle Clinical, coupled with knowledge of CDISC standards and, in many cases, a CCDM certification, is highly valued. Excellent attention to detail, strong organizational skills, and effective communication help distinguish top performers in this role. These abilities are crucial for ensuring compliant, high-quality data that supports successful clinical trials on a contractual or project basis.

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Contract Clinical Data Manager jobs near you
Infographic showing various Contract Clinical Data Manager job openings in Renton, WA as of August 2026, with employment types broken down into 71% Full Time, 14% Part Time, 5% Temporary, and 10% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $133,752 per year, or $64.3 per hour.

Associate Director, Clinical and Statistical Programming

Umoja Biopharma

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 22 days ago

Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.
Umoja Biopharma - Your Body. Your Hope. Your Cure.
POSITION SUMMARY
The Associate Director, Statistical Programming will be responsible for strategic planning, executing and quality checking of data programming and statistical analysis deliverables to support clinical trial conduction and prepare submission readiness package. This role provides technical and operational leadership to ensure compliant, high-quality analysis datasets, tables, listings, and figures (TLFs) in accordance with CDISC standards and FDA guidance. This role will operate as an individual contributor and is responsible for enhancing the statistical programming infrastructure of the Biometric department, building and leading a highly efficient data and matrixed statistical programming team (contractors, vendors, CROs, FTEs) over time.
This role will partner closely with Biostatistics, Clinical Data Management, Clinical Operations, and Regulatory Affairs to support submission readiness and successful regulatory interactions.
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days/week. We are open to remote within the US for the right candidate.
CORE ACCOUNTABILITIES
Specific responsibilities include:
  • Lead statistical programming activities for clinical trials and ensure the timely delivery of high-quality outputs throughout the full study life cycle.
  • Review clinical trial protocols, SAP, CRF designs, and EDC deployments, and provide input for EDC edit checks to enhance clinical trial data quality.
  • Guide and review outputs from CROs, which may encompass submission datasets, programs, and outputs to ensure the submission package (SDTM and ADaM specifications, SDTM and ADaM programs and datasets, Tables, Listings, and Figures (TLFs) outputs, define.xml, and reviewer guides, etc.) adheres to regulatory requirements and is compliant with CDISC standards.
  • Lead and support statistical programming activities for regulatory submissions including INDs, NDAs, and/or BLAs.
  • Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for downstream programming.
  • Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials, as well as ad hoc exploratory and publication analyses as required.
  • Mentor and provide technical oversight to statistical and data programmers and contractors.
  • Collaborate closely with biostatisticians, study physicians, data management, clinical operations, and safety review teams to review data or programming issues and improve the overall quality of clinical trial data.
  • Support internal and external audits, inspections, and regulatory inquiries related to statistical programming deliverables.
  • Assist the department head in building the infrastructure of the biometrics department, which may include creating macros and programs, TLF shells, departmental SOPs, and best practices for statistical programming and data traceability.

The successful candidate will have:
  • MS in biostatistics, statistics, computer science, or a closely related field, coupled with extensive quantitative analysis methodologies and statistical programming proficiency with a minimum of 10 years of experience in pharmaceutical companies or CROs is required.
  • At least 5 years of demonstrated leadership experience in projects and managing, mentoring, and developing teams.
  • A solid comprehension of statistical programming principles, advanced SAS programming expertise, extensive experience in the preparation of regulatory submission packages, and substantial knowledge of CDISC standards.
  • Exceptional attention to detail and a strong risk-mitigation mindset, a self-driven learner to continuous learning and updating programming skills and therapeutic area (TA) knowledge.
  • Excellent verbal, written, and interpersonal communication skills are mandatory for clear and efficient communication and collaboration with cross-functional teams, which may include clinical operations, data management, study physicians, statisticians, and medical writers.
  • A sound working knowledge of ICH, FDA, and GCP regulations and guidelines.

Preferred Qualifications:
  • Prior experience with NDA/ BLA submission and interaction with regulatory agencies is highly desirable, as is leading early and late-phase clinical trials.
  • Experience in immunology, hematology, or oncology clinical trials is preferred
  • Experience with using R in clinical analysis

Physical Requirements:
  • Ability to sit for prolonged periods of time
  • Ability to read, interpret, and review detailed technical documents, datasets, tables, listings, figures, and on-screen material
  • This role will ideally be based out of our Seattle, WA office and will be onsite 2 days/week
  • If this role is remote, the ability to travel up to 20% as needed

Salary Range: $185,100 - $228,700
Benefits Offerings
Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

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