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Cra Clinical Research Associate Jobs (NOW HIRING)

ICON

Clinical Research Associate

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

ICON

Clinical Research Associate

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

Novotech

Clinical Research Associate

$70K - $110K/yr

Role Summary The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate ...

Emmes

In-House CRA II

Rockville, MD · Remote

Primary Purpose The In-House Clinical Research Associate II (IH-CRA II) is responsible for assisting with operational activities supporting the site management and monitoring of clinical studies ...

ICON

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

ICON

Clinical Research Associate

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

ICON

Clinical Research Associate

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

ICON

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

ICON

Clinical Research Associate

Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial ...

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Cra Clinical Research Associate information

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

As of Jun 20, 2026, the average hourly pay for cra clinical research associate 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.

How much does a Clinical Research Associate get paid?

A Clinical Research Associate (CRA) typically earns between $60,000 and $110,000 annually, depending on experience, location, and the complexity of trials. Entry-level CRAs may start around $50,000, while experienced professionals with specialized skills can earn over $120,000. Salaries often include benefits and may increase with certifications like CCRP or RAC.

What are CRA Clinical Research Associates?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and Good Clinical Practice guidelines. They act as a bridge between the sponsor of a clinical trial and the sites where the trial is conducted, overseeing data collection, patient safety, and compliance. Their responsibilities include site visits, reviewing documentation, and ensuring accurate reporting of study results. CRAs play a critical role in advancing medical research by maintaining the integrity and quality of clinical studies.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, experience in clinical trial monitoring, and typically a bachelor's degree in a related field. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory requirements is essential, and certifications like ACRP or SOCRA are often advantageous. Strong attention to detail, organizational skills, effective communication, and adaptability help CRAs excel in coordinating studies and collaborating with diverse stakeholders. These skills ensure clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, safeguarding both data integrity and patient safety.

Which is better, CRC or CRA?

A Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance and data integrity, while a Clinical Research Coordinator (CRC) manages trial activities at the site level, including patient recruitment and data collection. Both roles are essential in clinical research, but CRAs typically work for sponsors or CROs and oversee multiple sites, whereas CRCs work directly with patients and site staff. The choice depends on whether you prefer site management or overseeing multiple trial sites, and both roles often require knowledge of Good Clinical Practice (GCP) and relevant certifications.

What are some common challenges faced by Clinical Research Associates (CRAs) when managing multiple clinical trial sites?

CRAs often juggle oversight of multiple clinical trial sites, which can present challenges such as coordinating visits, ensuring consistent protocol adherence, and managing varying site performance. Effective communication and strong organizational skills are crucial, as CRAs need to address site-specific issues, maintain accurate documentation, and ensure timely data collection. Additionally, adapting to diverse team dynamics and staying updated with regulatory requirements across sites are common aspects of the role. Employers typically provide training and support, but successful CRAs proactively develop strategies to manage these complexities.

What is a CRA Clinical Research Associate?

A CRA (Clinical Research Associate) is a professional responsible for monitoring clinical trials to ensure they are conducted according to protocol, Good Clinical Practice (GCP), and regulatory requirements. They oversee site activities, verify data accuracy, and communicate with investigators, often using electronic data capture systems. Strong attention to detail, knowledge of clinical trial processes, and relevant certifications are important for this role.

Is CRA an entry-level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, healthcare, or related fields. Entry-level roles in clinical research may include Clinical Trial Assistants or Coordinators, with CRAs often needing a bachelor's degree and relevant certifications such as ACRP or SOCRA to qualify for the role.

What is the difference between Cra Clinical Research Associate vs Clinical Trial Coordinator?

AspectCra Clinical Research AssociateClinical Trial Coordinator
CredentialsTypically requires a bachelor's degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonUsually holds a bachelor's degree in health sciences, nursing, or related field; certifications like CCRP are also beneficial
Work EnvironmentWorks primarily on-site at clinical trial sites, monitoring study progress and complianceCoordinates trial activities, manages schedules, and ensures protocol adherence, often working at trial sites or offices
Employer & IndustryEmployed by pharmaceutical companies, CROs, or research institutions in the clinical research industryEmployed by hospitals, research centers, or pharmaceutical companies to manage trial logistics

While both roles support clinical trials, Cra Clinical Research Associates focus on monitoring and compliance, whereas Clinical Trial Coordinators handle trial logistics and coordination. Both require relevant certifications and work in similar environments within the clinical research industry.

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Cra Clinical Research Associate jobs near you
Infographic showing various Cra Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 6% Full Time, 77% Part Time, 6% Temporary, and 11% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Senior Clinical Research Associate - CRA

C-Clinical San Diego

San Diego, CA • On-site, Remote

$65 - $90/hr

Contractor

Posted 4 days ago

Job description

Description
C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the San Diego region. This opportunity is ideal for professionals who enjoy working closely with investigative sites while maintaining strong oversight of complex clinical studies. The position includes both remote monitoring and on-site visits, creating a balanced environment that allows you to stay engaged with study teams while maintaining flexibility.
We are looking for individuals with a strong background in clinical monitoring and meaningful experience within central nervous system indications, such as neurology or psychiatry-related research. This position requires professionals who understand regulatory expectations, communicate effectively with site teams, and maintain a high level of attention to protocol compliance and data integrity.
C-Clinical is committed to advancing meaningful research that improves patient outcomes. Our team values collaboration, professionalism, and scientific integrity, and we welcome individuals who take pride in contributing to well-run clinical trials.
If you are a Senior CRA based in the greater San Diego area with strong CNS monitoring experience and are interested in working within a collaborative clinical research environment, we encourage you to apply.
Responsibilities
• Coordinate with study teams to support the successful initiation and execution of clinical trials
• Identify, evaluate, and qualify investigators and research sites within the San Diego region and surrounding areas
• Prepare and review essential documentation required for site initiation and regulatory readiness
• Conduct on-site monitoring visits and remote monitoring activities while maintaining detailed documentation of findings and follow-up actions
• Collaborate with Clinical Trial Managers and Project Managers to escalate site concerns and resolve operational challenges
• Review study data on an ongoing basis to identify discrepancies, missing information, or protocol deviations
• Support the full monitoring lifecycle, including pre-study visits, site initiation visits, routine monitoring visits, and close-out visits
• Verify that informed consent procedures and protocol requirements are properly followed to protect research participants
• Track and follow up on adverse events and serious adverse events while ensuring appropriate reporting procedures are followed
• Ensure the accuracy and integrity of case report form data through a comprehensive source document review
• Maintain compliance with study monitoring plans, standard operating procedures, and regulatory guidelines
• Participate in investigator meetings, project team meetings, and study-related teleconferences
• Maintain ongoing training related to ICH GCP, study protocols, and internal procedures
• Support regulatory documentation tracking, site performance evaluation, and study timeline adherence
Qualifications
• Five or more years of clinical research monitoring experience as a Clinical Research Associate
• At least three years of experience supporting studies in central nervous system indications, such as neurology or psychiatry-related therapeutic areas
• Minimum four years of experience working in contract-based CRA positions, such as independent contractor, consultant, or similar arrangements
• Experience conducting site monitoring visits and managing investigator site relationships
• Bachelor's degree from a four-year university, preferably in a scientific or health-related field
• Candidates with significant clinical research experience, nursing background, or relevant medical certifications may be considered in place of a traditional degree
• Ability to work as an independent vendor through an established corporation or LLC with appropriate business insurance
• Must have authorization to work in the United States
• Must be located within the greater San Diego area
• Availability to support studies for at least one year
• Strong communication skills in English and the ability to navigate complex clinical research discussions using medical terminology
• Professional communication skills with the ability to collaborate effectively across study teams and research sites
• Clinical research certifications, such as CCRA, CCRP, or similar credentials, are beneficial but not required

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