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Clinical Research Associate Jobs in Merced, CA (NOW HIRING)

JOB SUMMARY The Research Associate conducts testing procedures for project-based studies, such as shelf-life studies, inoculated challenge studies, process validation studies, etc., as described in ...

JOB SUMMARY The Research Associate conducts testing procedures for project-based studies, such as shelf-life studies, inoculated challenge studies, process validation studies, etc., as described in ...

JOB SUMMARY The Research Associate conducts testing procedures for project-based studies, such as shelf-life studies, inoculated challenge studies, process validation studies, etc., as described in ...

Amity is committed to research, development implementation, and dissemination of information ... The clinician's primary responsibility will be to provide quality clinical care through group ...

AOD Counselor III

Chowchilla, CA · On-site

$27 - $36.25/hr

Amity is committed to research, development implementation, and dissemination of information ... The clinician's primary responsibility will be to provide quality clinical care through group ...

Clinical Research Associate information

See Merced, CA salary details

$12

$43

$73

How much do clinical research associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical research associate in Merced, CA is $43.43, according to ZipRecruiter salary data. Most workers in this role earn between $30.48 and $55.58 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

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.

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

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 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.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

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.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Merced, CA? The most popular types of Clinical Research jobs in Merced, CA are:
What job categories do people searching Clinical Research Associate jobs in Merced, CA look for? The top searched job categories for Clinical Research Associate jobs in Merced, CA are:
What cities near Merced, CA are hiring for Clinical Research Associate jobs? Cities near Merced, CA with the most Clinical Research Associate job openings:
Infographic showing various Clinical Research Associate job openings in Merced, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,334 per year, or $43.4 per hour.

Research Associate

Certified Group

Turlock, CA • On-site

Full-time

Re-posted 9 days ago


Job description

JOB SUMMARY

The Research Associate conducts testing procedures for project-based studies, such as shelf-life studies, inoculated challenge studies, process validation studies, etc., as described in client proposal agreements. In addition, the Research Associate supports the work of other contract research laboratory personnel. The Research Associate also has elevated responsibility with regard to performing laboratory work that requires a higher level of technical expertise, including being a resource for operation of specialized instrumentation and for performing methods that are technically challenging. 

 ESSENTIAL RESPONSIBILITIES

  • Conducts all testing procedures in accordance with standard operating procedure and quality guidelines.
  • Accurately generates and transcribes pertinent data.
  • Interacts well with and serves as a training and troubleshooting resource to other department members.
  • Manages time and resources of their work and assists others in maximizing overall operational efficiency.
  • Can be relied upon to accurately execute scheduled tasks and assignments independently.
  • Proactively seeks ways to improve processes and better utilize departmental resources.
  • Acts as a resource for operation of specialized instrumentation and for obtaining thorough training on such instrumentation from the manufacturer.
  • Execute all pertinent scheduled preparation and testing procedures as described in project proposals.
  • Maintain meticulous records of procedures performed related to contract research studies.
  • Demonstrate proficiency in all testing procedures as assigned, including recording and maintaining accurate and timely results based on the analyses performed.
  • Learn new techniques and technologies as needed to complete project assignments.
  • Identify and communicate anomalous results and/or incongruent data sets with Department Manager/Supervisor.
  • Perform appropriate quality control tasks pertinent to the department including proper documentation and record keeping, in compliance with accreditation bodies.
  • Perform maintenance of laboratory equipment and instruments, including inspection, calibration, cleaning & sanitization, as directed.
  • Participate in special projects as assigned by the Department Manager/Supervisor


MINIMUM QUALIFICATIONS

  • B.S., preferably in Biology/Microbiology, and appropriate industry specific experience.
  • 2-5 years relevant laboratory experience or food production/testing environment experience.
  • Good conceptual basis in microbiology with proven ability to perform basic and advanced microbiology and molecular techniques.
  • Competence with effectively delivering and receiving oral or written communication.
  • Familiarity with FDA BAM, USDA MLG, CMMEF, APHA, and AOAC methodology.
  • Basic computer skills required.
  • Experience with Microsoft Office Suite applications, proficient with MS Excel.
  • LIMS experience preferable.
  • Manual dexterity.
  • Ability to distinguish colors, preferred.
  • Ability to stand for prolonged periods

PHYSICAL DEMANDS

  • Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components
  • Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens
  • Noise level varies from quiet to loud
  • Temperature varies from hot to cold
  • Color vision and depth perception
  • Interactive and fast-paced team oriented tasks
  • Overnight Travel may be required at the discretion of management
  • Regularly lift and/or move up to 25 pounds.

Schedule: Monday-Friday, 8:00am-4:30pm