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Clinical Data Manager Jobs in Bothell, WA (NOW HIRING)

May assist in clinical data review and query generation * Collaborates closely with Clinical Operations, Clinical Development, Biometrics, Clinical Data Management, Regulatory Affairs, Translational ...

Manage relationships with current data and technology partners -- ensuring they remain productive ... Assess gaps in our data offerings (SDoH, clinical depth, novel real-world sources, etc.), evaluate ...

Assess gaps in our data offerings (SDoH, clinical depth, novel real-world sources, etc.), evaluate potential partners, and manage the process end-to-end - from sourcing, and due diligence through ...

Performing clinical data review of data listings and summary tables, including query generation ... At least 1 year of experience managing industry sponsored pharmaceutical clinical trials as a ...

Performing clinical data review of data listings and summary tables, including query generation ... At least 1 year of experience managing industry sponsored pharmaceutical clinical trials as a ...

(Associate) Scientist, Health Data

Seattle, WA ยท On-site

$67K - $67K/yr

Curate, clean, and harmonize multi-omic, survey, biochemistry, and clinical data from international ... Strong attention to detail and record-keeping, and the ability to manage parallel workflows across ...

Curate, clean, and harmonize multi-omic, survey, biochemistry, and clinical data from international ... Strong attention to detail and record-keeping, and the ability to manage parallel workflows across ...

EDC Programmer

Redmond, WA ยท On-site

$100K - $150K/yr

Sitting in the Clinical Data Management (CDM) department, the EDCP works closely with Clinical Data Managers, Biostatistics, and other cross-functional study teams, leading electronic data capture ...

EDC Programmer

Redmond, WA ยท On-site

$100K - $150K/yr

Sitting in the Clinical Data Management (CDM) department, the EDCP works closely with Clinical Data Managers, Biostatistics, and other cross-functional study teams, leading electronic data capture ...

Interpret clinical data Review patient satisfaction function as first-level complaint resolution focal point. Participate in periodic management review. Operations: Arrange and conduct regular ...

Data Engineer IV

Seattle, WA

$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 ...

Data Engineer IV

Seattle, WA ยท 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 ...

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Clinical Data Manager information

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How much do clinical data manager jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for clinical data manager in Bothell, WA is $63.91, according to ZipRecruiter salary data. Most workers in this role earn between $50.53 and $76.06 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What degree do you need to be a Clinical Data Manager?

A Clinical Data Manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or health informatics. Many employers prefer candidates with a master's degree or additional certifications in clinical research or data management. Strong knowledge of database tools and regulatory standards is also important for the role.

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data management do?

A clinical data manager is responsible for designing, implementing, and maintaining systems to collect, clean, and analyze data from clinical trials. They ensure data accuracy, integrity, and compliance with regulatory standards using tools like electronic data capture (EDC) systems. This role requires attention to detail, knowledge of Good Clinical Practice (GCP), and often involves collaboration with research teams and data analysts.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills and familiarity with clinical trial software such as EDC systems.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for supporting regulatory submissions and ensuring trial integrity.
What are the most commonly searched types of Clinical Data jobs in Bothell, WA? The most popular types of Clinical Data jobs in Bothell, WA are:
What job categories do people searching Clinical Data Manager jobs in Bothell, WA look for? The top searched job categories for Clinical Data Manager jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Clinical Data Manager jobs? Cities near Bothell, WA with the most Clinical Data Manager job openings:
Infographic showing various Clinical Data Manager job openings in Bothell, WA as of July 2026, with employment types broken down into 93% Full Time, and 7% Contract. Highlights an 84% In-person, 6% Hybrid, and 10% Remote job distribution, with an average salary of $132,926 per year, or $63.9 per hour.
Senior Clinical Trial Manager

Senior Clinical Trial Manager

Umoja Biopharma

Seattle, WA โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 21 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 โ€“ Your Body. Your Hope. Your Cure.

POSITION SUMMARY

The Senior Clinical Trial Manager is primarily responsible for the operational management and oversight of Umoja's clinical studies. This individual will work closely with Clinical Operations leadership, Medical Director(s), other cross-functional team members, and designated CROs to ensure the successful completion of all clinical study activities and project deliverables within specified quality, time, and cost parameters.

The ideal candidate brings clinical operations expertise in biotech and the ability to thrive in a fast-paced, entrepreneurial environment.

This role is ideally based out of our Seattle, WA location and is onsite at least 2 days/week. We are open to remote work within the US for the right candidate.

CORE ACCOUNTABILITIES

Specific responsibilities include:

  • Ensures studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations and study specific manuals and procedures
  • Independently develop study timelines, key deliverables, and risk/mitigation strategies
  • Lead selection and performance management of CROs and other ancillary vendors during study start-up, conduct, and close-out
  • Plan and lead study team meetings
  • Lead the development of study materials (e.g., study plans, monitoring guidelines, site initiation visit materials, site tools and worksheets)
  • Contribute to the content and review of study documents (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, product administration guidelines)
  • Track and ensure optimization of site startup activities and activation, subject enrollment, data collection, and trial closeout
  • Ensure accurate and timely execution of site visit monitoring reports
  • Identify, select, and monitor performance of sites
  • Negotiate and manage the budgets and payments for sites
  • Develop and maintain strong working relationships with study investigators and site staff
  • Manage investigational product release packages and investigational product accountability
  • Coordinate with Clinical Supply Chain Operations regarding investigational product shipment to sites
  • Oversee the Trial Master File according to ICH- GCP and SOPs
  • May assist in clinical data review and query generation
  • Collaborates closely with Clinical Operations, Clinical Development, Biometrics, Clinical Data Management, Regulatory Affairs, Translational Medicine, Clinical Supply Chain, Pharmacovigilance, and Clinical Quality Assurance
  • Actively participate in and contribute to the development of department initiatives aimed at improving efficiency and best practices

The successful candidate will have:

  • Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 6 years of clinical operations experience in the pharmaceutical industry with at least 1 year experience managing industry-sponsored pharmaceutical clinical studies as a sponsor employee
  • Senior Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 8 years of clinical operations experience in the pharmaceutical industry with 3+ years' experience managing industry sponsored pharmaceutical clinical trials as a sponsor employee
  • Significant knowledge of GCP/ICH guidelines and the clinical development process
  • Ability to plan, organize and conduct clinical studies with minimum oversight
  • Significant experience managing CROs and other vendors and assessing performance
  • Experience leading, managing, or mentoring clinical operational staff and cross-functional teams
  • Strong organizational skills and the ability to balance changing priorities
  • Strong interpersonal and communication (written and verbal) skills
  • Demonstrated ability to work independently and as part of a multi-functional team
  • Able to solve problems under pressure
  • Self-motivated and able to work effectively in a matrix/team environment

Preferred Qualifications:

  • Experience supporting Phase 1 and 2 clinical trials is preferred
  • Oncology experience is highly preferred

Physical Requirements:

  • Ability to travel as needed (approximately 20%)
  • Ability to work onsite 2 days/week at our Seattle, WA office
  • Ability to sit for prolonged periods of time

Manager Level Salary Range: $125,000 - $150,000
Senior Manager Level Salary Range: $150,000 - $175,000

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.