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Remote Clinical Trial Manager Jobs in Bothell, WA

SDE II, Life Sciences Applied AI

Seattle, WA ยท On-site +1

$111K - $151K/yr

... manage day-to-day operations. We will accomplish this by accelerating our customers' businesses ... the entire clinical trial process, from planning, monitoring to regulatory submission. We are ...

SDE II, Life Sciences Applied AI

Seattle, WA ยท On-site +1

$111K - $151K/yr

... manage day-to-day operations. We will accomplish this by accelerating our customers' businesses ... the entire clinical trial process, from planning, monitoring to regulatory submission. We are ...

SDE II, Life Sciences Applied AI

Seattle, WA ยท On-site +1

$111K - $151K/yr

... manage day-to-day operations. We will accomplish this by accelerating our customers' businesses ... the entire clinical trial process, from planning, monitoring to regulatory submission. We are ...

SDE II, Life Sciences Applied AI

Seattle, WA ยท On-site +1

$111K - $151K/yr

... manage day-to-day operations. We will accomplish this by accelerating our customers' businesses ... the entire clinical trial process, from planning, monitoring to regulatory submission. We are ...

Showing results 41-60

Remote Clinical Trial Manager information

See Bothell, WA salary details

$32

$69

$107

How much do remote clinical trial manager jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for remote 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 is the difference between Remote Clinical Trial Manager vs Remote Clinical Research Associate?

AspectRemote Clinical Trial ManagerRemote Clinical Research Associate
CredentialsTypically requires a Bachelor's or higher in life sciences, with experience in trial managementUsually holds a Bachelor's in life sciences or related field, with certification in clinical research (e.g., CCRP)
Work EnvironmentOversees multiple sites, manages trial timelines, budgets, and teams remotelyMonitors trial sites, ensures protocol compliance, and collects data remotely
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

The Remote Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Remote Clinical Research Associate primarily monitors trial sites and data collection. Both roles require clinical research knowledge and often work remotely within the same industry sectors.

What does a remote clinical trial manager do?

Remote clinical trial managers monitor the process of clinical testing from home or another location outside of the office or lab. In this role, you may collaborate with the clinical project manager to create outlines for the trial, research relevant information from existing medical studies, and help ensure the scope of the testing is enough to move the product forward to the next phase. Products may include pharmaceuticals, medical devices, or other forms of medical treatments. Your job duties also involve creating strategies for efficient testing methods, checking that all tests comply with safety standards and current government regulations, documenting results, and supervising research assistants.

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

To thrive as a Remote Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, and project management, usually supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification are typically required. Exceptional organizational skills, proactive communication, and the ability to lead cross-functional teams remotely set top performers apart. These competencies are crucial for ensuring trial integrity, regulatory adherence, and seamless coordination across distributed teams.

How does a remote clinical trial manager typically collaborate with on-site study teams and stakeholders?

As a Remote Clinical Trial Manager, you will frequently coordinate with on-site study teams, investigators, and sponsors through virtual meetings, project management platforms, and regular reporting. Effective communication and proactive problem-solving are essential for ensuring trial milestones are met and regulatory requirements are followed, despite not being physically present. You may also oversee remote monitoring visits, address site queries, and facilitate cross-functional collaboration between data management, safety, and regulatory teams. This structure allows for flexibility while maintaining strong oversight and quality standards.

What is a remote clinical trial manager?

A Remote Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials from a remote location. They coordinate with various teams, ensure regulatory compliance, monitor trial progress, and manage budgets and timelines, all while working off-site. This role typically involves using digital tools to communicate, track data, and ensure the trial runs smoothly and efficiently. Remote Clinical Trial Managers are essential in facilitating clinical research, especially in decentralized or multi-site studies. They play a key role in ensuring that clinical trials meet both scientific and regulatory standards.

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

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

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

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

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

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

Infographic showing various Remote Clinical Trial Manager job openings in Bothell, WA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 18% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $145,364 per year, or $69.9 per hour.

Data Coordinator II

Fred Hutchinson Cancer Research Center

Seattle, WA โ€ข On-site, Remote

$27.01 - $38.45/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago


Job description

Overview

Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.

With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world's leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world's deadliest diseases and make life beyond cancer a reality.

At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.

Theย Data Coordinator IIย monitors data collection and its adherence to protocols andย is responsible forย the collection, coordination, processing, and quality control of clinical trial data.ย 

Most Fred Hutch jobs requiresomeon-campus work. However, there may be flexibility for certain positions. Please check with theย recruiterย if you are an out-of-state applicant interested only in working outside of the Seattle area.ย 

Postion can be offered fully remote:

Responsibilities
  • Work with the research team and providers to collect, abstract, and code complex clinical data and information from multiple sources (medical records, research records, etc.) for research subjects.ย 
  • Code andย record saidย information into various study-specific electronic data-capture systems.ย 
  • Resolve and answer data queries with minimal errors.ย 
  • Maintain databases for research studies.ย 
  • Demonstrate understanding of research study operational flow.ย 
  • Assistย with development of study-specific or program data acquisition forms.ย 
  • Partner with research coordinator and/or sponsor representatives to review and correct data recorded in the case report forms.ย 
  • Request medical records from outside medical facilities.ย 
  • Track andย maintainย research subject schedules based on complex protocol-specific requirements, and work with clinic staff support services and research team members to ensure subject research assessments are planned forย required/appropriate time points.ย 
  • May interact with research subjects, study team members, or sponsor contactsย in order toย obtain andย submitย required study dataย and forย resolution of study-specific queries.ย 
  • Additionalย duties as assigned.ย 
Qualifications

MINIMUM QUALIFICATIONS:

  • BA/BS, RRA (Registered Records Administrator), ART (Accredited Records Technician), or two year degree in the medical field.
  • Two years of experience in medical records, cancer registry, or related field.
  • Strong computer skills and experience working with databases.
  • Strong verbal and written communication skills.
  • Medical terminology.

PREFERRED QUALIFICATIONS:

  • Experience working in oncology research and with medical terminology or electronic medical record preferred.ย 
  • CCRP or CCRC accreditation preferred.ย 
  • Strong attention to detail and ability to multi-task, organize and prioritize multiple projects.ย 
  • Ability to work effectively with colleagues, research subjects, and study sponsor representatives.ย 
  • Demonstrated ability to work independently, under supervision, and be a team player.ย 
  • Ability to adapt and respond appropriately to competing priorities in a fast-paced environment.ย 

The hourly pay range for this position is from $27.01 to $38.45 and pay offered will be based on experience and qualifications.Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).

Additional InformationWe are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.Employment Type: FULL_TIME