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Clinical Research Associate Jobs (NOW HIRING)

Piper Companies

Clinical Research Associate

Chicago, IL · Hybrid

$120K - $135K/yr

Piper Companies is actively seeking Clinical Research Associates to join a toptier CRO with a proven track record of excellence, trusted by global pharma and biotech partners. This position is fully ...

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How much do clinical research associate jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for 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 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 be challenging for those without related experience or 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 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.
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Who are the top companies hiring for Clinical Research Associate jobs? The top employers for Clinical Research Associate jobs are:
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Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 73% Full Time, 16% Part Time, and 9% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.
Clinical Research Assoc III

Clinical Research Assoc III

Tranquil Clinical Research

Webster, TX • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Clinical Research Associate III

The Clinical Research Associate III will play a pivotal role in the management and oversight of clinical trials, ensuring that they are conducted in compliance with regulatory requirements and company standards. This position is responsible for monitoring study sites, collecting and analyzing data, and ensuring the integrity of the research process. The successful candidate will collaborate with cross-functional teams to facilitate the smooth execution of clinical studies, contributing to the advancement of medical knowledge and patient care. Additionally, the Clinical Research Associate III will provide training and mentorship to junior staff, fostering a culture of excellence and continuous improvement. Ultimately, this role is essential in driving the success of clinical research initiatives that can lead to innovative healthcare solutions.

Minimum Qualifications:

  • Bachelor's degree in life sciences, nursing, or a related field.
  • At least 3 years of experience in clinical research monitoring.
  • Must have oncology experience
  • Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
  • Trip report review experience
  • PSSV, SIV, IMV, COV and TMF reconciliation experience
  • Onsite monitoring experience with at least 3 years

Preferred Qualifications:

  • Master's degree in a relevant field.
  • Experience with electronic data capture (EDC) systems.
  • Certification as a Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC).

Responsibilities:

  • Monitor clinical trial sites to ensure compliance with study protocols and regulatory requirements.
  • Conduct site visits, perform source document verification, and ensure data integrity.
  • Collaborate with investigators and site staff to facilitate the smooth execution of clinical studies.
  • Prepare and review study-related documentation, including protocols, informed consent forms, and reports.
  • Provide training and support to junior clinical research associates and other team members.

The required skills for this position include strong analytical abilities, which are essential for evaluating clinical data and ensuring compliance with protocols. Excellent communication skills are necessary for effectively collaborating with site staff and presenting findings to stakeholders. Attention to detail is critical in monitoring clinical trials and verifying data accuracy. Preferred skills, such as proficiency in EDC systems, enhance the efficiency of data collection and management processes. Overall, a combination of these skills will enable the Clinical Research Associate III to contribute significantly to the success of clinical research projects.

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