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Clinical Research Associate Jobs in Rohnert Park, CA

Buck Institute

Clinical Project Manager

Novato, CA · On-site

$90K - $100K/yr

Lead, mentor, train, and support Clinical Research Associates, ensuring training, delegation, workload distribution, and back-up coverage are appropriately managed and documented. * Coordinate ...

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Clinical Research Associate information

See Rohnert Park, CA salary details

$13

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$77

How much do clinical research associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research associate in Rohnert Park, CA is $45.56, according to ZipRecruiter salary data. Most workers in this role earn between $31.97 and $58.32 per hour, depending on experience, location, and employer.

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 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 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 work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

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 in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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What are the most commonly searched types of Clinical Research jobs in Rohnert Park, CA?

The most popular types of Clinical Research jobs in Rohnert Park, CA are:

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The top searched job categories for Clinical Research Associate jobs in Rohnert Park, CA are:

What cities near Rohnert Park, CA are hiring for Clinical Research Associate jobs?

Cities near Rohnert Park, CA with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Rohnert Park, 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 $94,756 per year, or $45.6 per hour.

Clinician-Research Associate TrueNorth Health Foundation

Healthpromoting

Santa Rosa, CA • On-site

$60 - $80/hr

Other

Posted 4 days ago

Job description

Clinician–Research Associate TrueNorth Health Foundation

The TrueNorth Health Foundation is looking for a Clinician–Research Associate to join our residential clinical program in medically supervised prolonged water-only fasting and whole-plant-food, SOS‑free refeeding.

This role is designed for a clinician — or clinician‑in‑training — with at least a year of research experience who wants genuine mentorship in fasting and refeeding medicine alongside the opportunity to contribute meaningfully to projects that document, curate, and advance the clinical science of fasting.

Key Responsibilities Clinical training
  • Participate in daily patient monitoring and documentation workflows under senior clinician supervision
Case reports
  • Identify novel cases with attending clinicians
  • Coordinate with patients and clinicians to confirm timelines, fill gaps, and support follow‑up
  • Extract and organize case data — history, clinical course, vitals, labs, medications, adverse events, outcomes — into a structured case file
  • Research the relevant condition and fasting/refeeding literature to contextualize each case
  • Draft first versions of case reports for internal review and peer‑reviewed submission, CARE‑guidelines aligned
  • Help maintain the Foundation's fasting literature database,
  • Review and improve existing records: fix metadata, attach PDFs, standardize tagging by condition, protocol, duration, outcomes, and adverse events
  • Add new publications with brief structured annotations covering study design, population, protocol, key findings, and limitations
Systems and workflow
  • Collaborate with the research team to define and apply consistent database standards: required fields, controlled vocabulary, PDF naming and storage
  • Build and maintain a case report pipeline: nomination criteria, tracking system, data‑extraction template, follow‑up checklist, and internal review steps
Qualifications Required
  • Clinician (MD/DO/ND/PA/NP/RN/DC) or enrolled in a clinical degree program
  • 1–2 years of research experience — clinical, thesis, academic lab, or equivalent
  • Strong writing skills and a careful, methodical approach to clinical records and data abstraction
  • Able to work on‑site in a residential clinical environment
Preferred
  • Experience with case reports, chart reviews, or manuscript drafting
  • Literature searching, evidence synthesis, or reference management (Zotero, EndNote)
  • A demonstrated interest in nutritional medicine

Location: TrueNorth Health Center, Santa Rosa, CA. On‑site, residential setting. Full‑time. Competitive salary + housing and whole‑plant‑food, SOS‑free meals provided.

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