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Clinical Research Associate Jobs in Riverside, CA

JenaValve

Senior Associate, Clinical Research

Irvine, CA · On-site

$95K/yr

Senior Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The ...

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The ...

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The ...

Johnson & Johnson

Clinical Research Leader

Irvine, CA · On-site +1

Interfaces, collaborates and oversees Clinical Research Associates (CRAs); * Oversees and supports the development and execution of Investigator agreements and trial payments; * Is responsible for ...

Jj

Clinical Research Leader

Irvine, CA · On-site +1

Interfaces, collaborates and oversees Clinical Research Associates (CRAs); * Oversees and supports the development and execution of Investigator agreements and trial payments; * Is responsible for ...

Johnson and Johnson

Clinical Research Leader

Irvine, CA · On-site +1

Interfaces, collaborates and oversees Clinical Research Associates (CRAs); * Oversees and supports the development and execution of Investigator agreements and trial payments; * Is responsible for ...

Jj

Clinical Research Leader, Neurovascular

Irvine, CA · On-site +1

Interfaces, collaborates and oversees Clinical Research Associates (CRAs); * Oversees and supports the development and execution of Investigator agreements and trial payments; * Is responsible for ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Riverside, CA

Clinical Research Associate information

See Riverside, CA salary details

$12

$42

$72

How much do clinical research associate jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for clinical research associate in Riverside, CA is $42.91, according to ZipRecruiter salary data. Most workers in this role earn between $30.10 and $54.90 per hour, depending on experience, location, and employer.

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 still be challenging for those without prior experience or specialized training.

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.

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 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.

What is the work of clinical research associate?

A clinical research associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, regulations, and Good Clinical Practice standards. They coordinate with investigators, review trial data, and ensure compliance, often using clinical trial management systems. CRAs typically require knowledge of regulatory requirements and may need certification or training in clinical research.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an entry-level to mid-level position in clinical research, often requiring a bachelor's degree in a related field and some experience or training in clinical trials. Entry-level CRAs may need to complete training on Good Clinical Practice (GCP) and may start as clinical trial assistants or coordinators before advancing to CRA roles.

How do you become a clinical research associate?

To become a clinical research associate (CRA), candidates typically need a bachelor's degree in a health-related field such as life sciences, nursing, or pharmacy. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and certification from organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. CRAs often undergo on-the-job training and may pursue additional certifications to advance their careers.

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

Senior Associate, Clinical Research

JenaValve

Irvine, CA • On-site

$95K/yr

Full-time

Posted 19 days ago

Job description

Job Title: Senior Associate, Clinical Research
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Director, Clinical Affairs
Job Location & Environment: Irvine, CA, Corporate Office
Job Description Summary: The Senior Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations.
Job Responsibilities:
  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities - i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Generate queries to resolve data issues and apply corrections to database.
  • Act as a point person for all data related to clinical group, and to provide data to cross-functional departments.
  • Conduct EDC training to external teams and sites.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates).
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives.
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support co-monitoring of local sites on an as-needed basis.

Required Education and Experience:
  • 2+ year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.

Skills and Abilities Required for This Job:
  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Deep knowledge of GCPs governing the conduct of clinical trials; working knowledge of Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines.
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.

Physical Requirements:
  • Ability to travel up to 20% time.

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