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Study Manager Jobs in Seattle, WA (NOW HIRING)

Senior Clinical Trial Manager

Seattle, WA · On-site

$150K - $175K/yr

Ensures studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines ... Lead selection and performance management of CROs and other ancillary vendors during study start-up ...

Research Associate

Everett, WA · On-site

$22 - $28/hr

The role involves managing multiple studies and ensuring high levels of documentation and compliance with protocols. Key Responsibilities * Follow SOPs and Protocols to perform procedures on study ...

Explain study parameters and obtain informed consent. Screen subjects and conduct interviews ... Manager. * Two years of college-level course work in a relevant academic area AND one year of ...

Project Manager II

Seattle, WA · On-site

$88K - $133K/yr

Serve as project/study liaison, representing the project/study to other Center departments, funding ... Manage internal and external stakeholder expectations. * Triage project issues and ensure solutions ...

Clinic Scheduler

Tacoma, WA · On-site

$21.31 - $38.59/hr

Scheduler - General & Specialty Cardiology Cardiac Study Center/ Pulse Heart Institute, Tacoma, WA ... Key responsibilities include managing appointments across various departments, ensuring smooth ...

Clinic Scheduler

Tacoma, WA · On-site

$21.31 - $38.59/hr

Scheduler General & Specialty Cardiology Cardiac Study Center/ Pulse Heart Institute, Tacoma, WA ... Key responsibilities include managing appointments across various departments, ensuring smooth ...

Cardiac Device Monitor Tech

Tacoma, WA · On-site

$24.06 - $38.82/hr

Managing monitor equipment inventory, maintenance, and staff training on device usage. * Supporting various clinic locations as needed and participating in educational programs. Cardiac Study Center ...

Clinic Scheduler

Tacoma, WA

$21.31 - $38.59/hr

Scheduler - General & Specialty Cardiology Cardiac Study Center/ Pulse Heart Institute, Tacoma, WA ... Key responsibilities include managing appointments across various departments, ensuring smooth ...

Medical Assistant

Tacoma, WA · On-site

$22.96 - $41.61/hr

Manage medical supply inventory, restocking exam rooms as needed. * Assist patients with any questions they may have. * Adhere to HIPAA and OSHA standards at all times Cardiac Study Center/ Pulse ...

Manage medical supply inventory, restocking exam rooms as needed. * Assist patients with any questions they may have. * Adhere to HIPAA and OSHA standards at all times Cardiac Study Center/ Pulse ...

Cardiac Device Monitor Tech

Auburn, WA · On-site

$24.06 - $38.82/hr

Managing monitor equipment inventory, maintenance, and staff training on device usage. * Supporting various clinic locations as needed and participating in educational programs. Cardiac Study Center ...

Clinic Scheduler

Tacoma, WA · On-site

$21.31 - $38.59/hr

Scheduler - General & Specialty Cardiology Cardiac Study Center/ Pulse Heart Institute, Tacoma, WA ... Key responsibilities include managing appointments across various departments, ensuring smooth ...

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Showing results 1-20

Study Manager information

See Seattle, WA salary details

$27.9K

$67.8K

$132.1K

How much do study manager jobs pay per year?

As of Jul 16, 2026, the average yearly pay for study manager in Seattle, WA is $67,779.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,800.00 and $78,000.00 per year, depending on experience, location, and employer.

How does a Study Manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

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

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What does a Study Manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
What are the most commonly searched types of Study jobs in Seattle, WA? The most popular types of Study jobs in Seattle, WA are:
Senior Clinical Trial Manager

Senior Clinical Trial Manager

Umoja Biopharma

Seattle, WA • On-site

$150K - $175K/yr

Other

Re-posted 22 days ago


Job description

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