ZipRecruiter

Log In

1

Clinical Research Associate Cro Jobs (NOW HIRING)

NWRPros

Clinical Research Associate

Seattle, WA · On-site

$115K - $145K/yr

As Clinical Research Associate (CRA) you will be primarily responsible for the operational ... Assisting Clinical Trial Manager in managing CRO partners and other vendors * Working closely with ...

Natera

OR · On-site

The Senior Clinical Research Associate is responsible for the overall operational execution of ... and CRO databases, for studies where Natera functions as a Clinical Research Site. * Update ...

410 ICR United States USA

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - East Region ICON is a global health ... CRO industry * Experienced monitoring Oncology specifically Myelofibrosis clinical trials.

Icon plc

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global health ... CRO industry * Experienced monitoring Oncology specifically Myelofibrosis clinical trials.

Icon plc

Sr. Clinical Research Associate

Washington, DC · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global health ... CRO industry * Experienced monitoring Oncology specifically Myelofibrosis clinical trials.

Emmes

Sr. Clinical Research Associate

Rockville, MD · Hybrid

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites ...

previous pagenext page

Showing results 21-40

All JobsClinical Research Associate Cro Jobs

Clinical Research Associate Cro information

See salary details

$12

$41

$69

How much do clinical research associate cro jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical research associate cro in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

More about Clinical Research Associate Cro jobs
What cities are hiring for Clinical Research Associate Cro jobs? Cities with the most Clinical Research Associate Cro job openings:
What states have the most Clinical Research Associate Cro jobs? States with the most job openings for Clinical Research Associate Cro jobs include:
What job categories do people searching Clinical Research Associate Cro jobs look for? The top searched job categories for Clinical Research Associate Cro jobs are:
Clinical Research Associate Cro jobs near you
Infographic showing various Clinical Research Associate Cro job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate

NWRPros

Seattle, WA • On-site

$115K - $145K/yr

Full-time

Re-posted 5 days ago

Job description

Our client is an exciting 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. The Company has developed a proprietary technology designed to facilitate targeted drug delivery of both existing and novel drugs.
The current target application is currently in a Phase 1b/2 trial.Potential pipeline indications include candidates for other indications, each designed to improve on the activity and tolerability of currently approved drugs.
Location:Full Time; Seattle based
Scope: As Clinical Research Associate (CRA) you will be primarily responsible for the operational management and oversight of the client's 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.

Apply