ZipRecruiter

Log In

1

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

Aurion Biotech Inc.

Clinical Study Manager

Seattle, WA · On-site

$95K - $113K/yr

Director, Clinical Trial Management SALARY RANGE: $95,000 to $113,000 ABOUT THE POSITION Aurion Biotech is a clinical-stage biotechnology company dedicated to restoring vision to millions of patients ...

Doist

Director, Clinical Operations

Seattle, WA · On-site

$215 - $240/hr

Th is individual will manage trial budgets, vendor selection, and risk mitigation while contributing technical input to key clinical documents. This individual will also mentor staff, foster strong ...

next page

Showing results 1-20

All JobsClinical Trial JobsClinical Trial Manager JobsClinical Trial Manager Jobs in Bothell, WA

Clinical Trial Manager information

See Bothell, WA salary details

$32

$69

$107

How much do clinical trial manager jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical trial manager in Bothell, WA is $69.89, according to ZipRecruiter salary data. Most workers in this role earn between $56.68 and $78.75 per hour, depending on experience, location, and employer.

What does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

What are the key skills and qualifications needed to thrive as a clinical trial manager, and why are they important?

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.
More about Clinical Trial Manager jobs

What are the most commonly searched types of Clinical Trial jobs in Bothell, WA?

The most popular types of Clinical Trial jobs in Bothell, WA are:

What are popular job titles related to Clinical Trial Manager jobs in Bothell, WA?

For Clinical Trial Manager jobs in Bothell, WA, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Manager jobs in Bothell, WA look for?

The top searched job categories for Clinical Trial Manager jobs in Bothell, WA are:

What cities near Bothell, WA are hiring for Clinical Trial Manager jobs?

Cities near Bothell, WA with the most Clinical Trial Manager job openings:

Clinical Trial Manager jobs near you
Infographic showing various Clinical Trial Manager job openings in Bothell, WA as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $145,364 per year, or $69.9 per hour.

Senior Clinical Trial Manager

Umoja Biopharma

Seattle, WA • On-site, Remote

Full-time

Re-posted 3 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 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.