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Clinical Research Associate Jobs in Bothell, WA (NOW HIRING)

Icon plc

Senior CRA

Seattle, WA

$110.52K - $138.15K/yr

Sr Clinical Research Associate - Ophthalmology - West ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving ...

People With Chemistry

CRA

Seattle, WA

Clinical Research Associate (CRA) Meet Life Sciences is representing a client seeking a Clinical Research Associate (CRA) to support the operational management and oversight of clinical study ...

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Clinical Research Associate information

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$13

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$77

How much do clinical research associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical research associate in Bothell, WA is $45.97, according to ZipRecruiter salary data. Most workers in this role earn between $32.26 and $58.85 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may be challenging for those without related experience or training.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Bothell, WA? The most popular types of Clinical Research jobs in Bothell, WA are:
What are popular job titles related to Clinical Research Associate jobs in Bothell, WA? For Clinical Research Associate jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Bothell, WA look for? The top searched job categories for Clinical Research Associate jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Clinical Research Associate jobs? Cities near Bothell, WA with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you

Clinical Research Associate

Eupraxia Pharmaceuticals Inc.

Seattle, WA

$115K - $145K/yr

Other

Posted 8 days ago

Job description

Clinical Research Associate

Eupraxia is a clinical-stage biotechnology company focused on developing locally delivered, extended-release products that have the potential to address therapeutic areas with high unmet medical need. DiffuSphereâ„¢, a proprietary, polymer-based micro-sphere technology, is designed to facilitate targeted drug delivery of both existing and novel drugs. The technology is designed to support an extended duration of effect and delivery of drugs in a hyper-localized fashion, targeting only the tissues that physicians want to treat. We believe the potential for fewer adverse events may be achieved through the precision targeting and the stable and flat delivery of the active ingredient when using the DiffuSphereâ„¢ technology, versus the peaks and troughs seen with more traditional drug delivery methods. The precision of Eupraxia's DiffuSphereâ„¢ technology platform has the potential to augment and transform existing FDA-approved drugs to improve their safety, tolerability, efficacy and duration of effect. The potential uses in therapeutic areas may go beyond pain and inflammatory gastrointestinal disease, where Eupraxia currently is developing advanced treatments, also to be applicable in oncology, infectious disease and other critical disease areas.

As our Clinical Research Associate (CRA) you will be primarily responsible for the operational management and oversight of Eupraxia clinical study's monitoring.

Travel requirement: Must be willing to travel domestically and internationally (approximately 20-25%), as needed

Reports to: SVP of Clinical Operations

Primary Responsibilities:

  • Assisting Clinical Trial Manager in ensuring trials are initiated efficiently, completed on time, within budget and conducted in compliance with SOPs, regulations, and ICH/GCP guidelines
  • Assisting Clinical Trial Manager in managing CRO partners and other vendors
  • Working closely with and providing training to CRO staff, study site staff, and field-based CRAs
  • Overseeing, conducting, and/or co-monitoring site qualification, study initiation, interim monitoring, and close out visits and completing associated reports
  • Developing and/or assisting in the development of trial materials (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, monitoring guidelines, site initiation visit materials, site tools and worksheets, product administration guidelines)
  • Reviewing monitoring reports and monitoring visit letters written by CRO CRAs
  • Driving CRO and trial sites with study startup activities, including IRB/IEC submissions and ensuring collection and review of required essential documents
  • Creating, monitoring, and sharing key performance metrics with study teams
  • Reviewing completed CRFs and data listings for accuracy, overseeing data discrepancy management, and performing associated training/retraining to site staff and CRAs as needed
  • Developing strong and effective working relationships within Clinical Operations and other functional departments and CROs

Job Qualifications and Requirements:

  • BS/BA in life sciences or related discipline
  • 5+ years pharma/biopharma industry experience, preferably in a sponsor-side role
  • 1+ years of active, independent, on-site monitoring experience for all types of visits
  • Strong working knowledge of FDA and ICH/GCP regulations and guidelines
  • Thorough knowledge of clinical monitoring procedures
  • Strong interpersonal, communication (written and verbal), and organizational skills
  • Excellent analytical and assessment skills, judgment, and problem-solving skills

Salary Range: $115,000 - $145,000 annually depending on education and relevant experience.

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