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Cra Clinical Research Associate Jobs (NOW HIRING)

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

Are you passionate about clinical research and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

Are you passionate about clinical research and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

Are you passionate about clinical research and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

CRA II or Senior CRA-US-Remote ICON is a global healthcare intelligence and clinical research ... ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical ...

ICON

Clinical Research Associate

Senior Clinical Research Associate - Oncology ICON is a global healthcare intelligence and clinical ... As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Primary Purpose The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted ...

Icon plc

CRA II and Senior CRA

Lawrence, KS · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and ...

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All JobsCra Clinical Research Associate Jobs

Cra Clinical Research Associate information

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$12

$41

$69

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

As of Jul 15, 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.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive due to the specialized skills required, such as knowledge of Good Clinical Practice (GCP) and clinical trial processes. Candidates often need relevant education, certifications, and experience in clinical research to improve their chances of obtaining a CRA role.

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 $60,000, while experienced professionals or those working in high-cost areas can earn over $100,000. Certifications and familiarity with clinical trial management systems can also influence salary levels.

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.

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 does a clinical research associate do in CRA?

A Clinical Research Associate (CRA) monitors clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They conduct site visits, review data for accuracy, and communicate with investigators to ensure trial integrity and patient safety.

Is CRA an entry level job?

A CRA (Clinical Research Associate) 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 assistant or coordinator positions, with CRA roles often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications or training.

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.

More about Cra Clinical Research Associate jobs
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Cra Clinical Research Associate jobs near you

Clinical Research Associate

CTTX Health

Cambridge, MA • On-site

Contractor

Posted 19 days ago

Job description

Are you passionate about clinical research and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) that's advancing innovative therapies in neuroscience.
What You'll Do:
  • Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality standards.
  • Review and verify study data for accuracy and completeness.
  • Collaborate with site staff and cross-functional teams to solve challenges and keep trials on track.
  • Identify and escalate any protocol deviations, safety concerns, or data issues.

Requirements
What We're Looking For:
  • Bachelor's in Life Sciences, Nursing, Pharmacy, or related field (advanced degree a plus).
  • 3+ years of CRA or site monitoring experience.
  • Strong knowledge of ICH-GCP and FDA regulations.
  • Excellent communication, organization, and problem-solving skills.
  • Willingness to travel as needed (up to 50-75%).

Extra Credit:
  • Experience with CNS or rare-disease trials.

Benefits
Amazing benefits package starting day one!

Apply