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

Medical Assistant Phlebotomist certification for Washington State, or readiness to obtain it ... Comfort working with clinical/laboratory data and research data systems; experience with EDC ...

Medical Assistant Phlebotomist certification for Washington State, or readiness to obtain it ... Comfort working with clinical/laboratory data and research data systems; experience with EDC ...

May provide clinical back-up to other Research Coordinators and Research Assistants. Primary Duties: 1. Recruits, interviews and screens potential subjects to determine eligibility on trial under ...

May provide clinical back-up to other Research Coordinators and Research Assistants. Primary Duties: 1. Recruits, interviews and screens potential subjects to determine eligibility on trial under ...

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Clinical Research Assistant information

See Bothell, WA salary details

$9

$25

$51

How much do clinical research assistant jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical research assistant in Bothell, WA is $25.39, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $29.04 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistants often start with little or no experience, as entry-level positions may provide on-the-job training. Relevant skills such as attention to detail, basic knowledge of medical terminology, and familiarity with data entry or research protocols can help candidates qualify for these roles. Certifications like Good Clinical Practice (GCP) can also improve job prospects for those new to the field.
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 job categories do people searching Clinical Research Assistant jobs in Bothell, WA look for? The top searched job categories for Clinical Research Assistant jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Clinical Research Assistant jobs? Cities near Bothell, WA with the most Clinical Research Assistant job openings:
Infographic showing various Clinical Research Assistant job openings in Bothell, WA as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 22% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $52,810 per year, or $25.4 per hour.

Clinical Research Coordinator I

ERA Health Research

Redmond, WA • On-site

$30 - $32.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

ERA Health Research is seeking a full-time Clinical Research Coordinator I to join our Clinical Operations team in Redmond, WA. The Clinical Research Coordinator I coordinates all aspects of clinical trials, ensuring that trials are conducted according to ethical, regulatory, and scientific standards while maintaining participant safety and data integrity.

DUTIES & RESPONSIBILITIES

  • Identify objectives, endpoints and outcome measures for a given clinical trial.
  • Implement protocol and any protocol amendments according to GCP, verifying that only IRB/IEC approved versions of study documents are being used.
  • Schedule, coordinate, and prepare documents, equipment, facilities for site initiation visits.
  • Complete training and interpret a study implementation plan for relevant items that impact the tasks and activities the coordinator should prioritize for a given trial.
  • Ensure consistency between the sites’ standard operating procedures (SOPs) and the study requirements.
  • Identify all study supplies needed for a given clinical trial, assess and reconcile inventory to ensure adequate supplies throughout the trial.
  • Develop and organize trial management tools such as subject study calendar, source documents, and retention materials to enhance subject compliance.
  • Complete pre-screening, screening and enrollment logs and forms in an accurate and timely manner.
  • Coordinate with regulatory, recruitment, and clinical staff to schedule patient visits.
  • Complete informed consent and randomization of subjects accurately and according to the protocol and SOPs to ensure appropriate inclusion of subjects.
  • Support and manage investigational product, including labeling, preparing and dispensing.
  • Collect, ship, and store specimens according to requirements.
  • Manage, educate and communicate with subjects throughout the trial, including communicating about compliance with the visit schedule, protocol procedures, diary completion, and discontinuation.
  • Complete study communications, comments, and logs in an accurate and timely manner, including basic clinical data entry into Electronic Data Capture (EDC) systems, and documenting and reporting any unanticipated problems, deviations and/or safety related issues following GCP.
  • Schedule, coordinate, and prepare documents for monitoring visits; review monitoring visit follow-up reports / letters and perform requested post-visit activities, including resolving queries in an accurate and timely manner.
  • Help with the preparation, organization, and maintenance of regulatory documents and study binders.
  • Train new team members on clinical research skills to enhance competency.
  • Travel to and from other company sites as needed to perform job responsibilities.
  • In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.

QUALIFICATIONS

Required:

  • 1-2 years of Clinical Research Experience
  • Basic understanding of scientific and medical terminology
  • Meticulous attention to detail, with ability to follow complex instructions and protocols precisely
  • Strong organizational and problem-solving skills
  • Team player able to effectively self-reflect, communicate, and collaborate across teams
  • Good written and verbal communication skills
  • Ability to obtain and maintain an active, unrestricted Washington State Medical Assistant-Registered (MA-R) AND Medicals Assistant-Phlebotomist (MA-P) credentials. ERA will assist the selected candidate with obtaining the initial credentials and will cover initial and renewal credentialing fees. Employees are responsible for maintaining active credentials throughout employment
  • Current Basic Life Support (BLS) certification is not required at the time of hire. Candidates who already hold a current BLS certification may provide documentation upon hire Employees without current BLS certification must obtain certification within the first 90 days of employment. The employer will pay the initial certification fee, and employees are responsible for maintaining current BLS certification throughout employment
  • Proficient with basic computer software (MS Office)

Pay & benefits

Pay Range: $30.00/hourly - $32.50/hourly


Pay is based upon candidate experience and qualifications, as well as market and business considerations

ERA Health Research provides eligible employees with an opportunity to enroll in a comprehensive benefits package which includes:

  • Medical, dental, and vision insurance
  • Flexible Spending Account (FSA) and Health Savings Account (HSA) options
  • 401k Retirement Savings Plan
  • Paid time off (PTO) starting at 10 days per year and 1 hour of sick leave for every 40 hours worked.
  • 2 Floating Holidays per year