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CRA

Forest City, NC

CRA POSITION TITLE: CLINICAL RESEARCH ASSOCIATE (CRA) REPORTS TO: Project Manager LOCATION: MADRID (SPAIN) MISSION: Ensure that clinical trials are conducted, documented, and reported in full ...

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410 ICR United States USA

CRA II and Senior CRA

Houston, TX · Remote

$91K - $114K/yr

CRA II or Senior CRA (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

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CRA II and Senior CRA

Lawrence, KS · Remote

$91K - $114K/yr

CRA II or Senior CRA (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

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CRA II and Senior CRA

Downers Grove, IL · Remote

$91K - $114K/yr

CRA II or Senior CRA (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Cathay Bank

CRA Administration Officer (NE)

El Monte, CA · On-site

$33.65 - $48.08/hr

Represent the Bank and CRA team at various community events and bank sponsored events. * Along with the SVP, Director of Community Development, be actively involved in the annual Risk Control Self ...

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CRA II and Senior CRA

Salt Lake City, UT · Remote

$91K - $114K/yr

CRA II or Senior CRA (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 3 clinical trial in the Kidney transplant therapeutic area. The ideal candidate will have a ...

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How much do cra jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for cra 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.

What Is a CRA?

A CRA, or clinical research associate, is an investigator who makes sure that medical research follows protocols and meets ethical standards. The primary responsibilities of CRAs include monitoring clinical research trials to verify the accuracy of the trial data as well as the safety and well-being of patients. To carry out these duties, CRAs visit the clinical sites where a study takes place, such as hospitals and other facilities, review documents, and observe trial proceedings.

What are the key skills and qualifications needed to thrive as a Chartered Accountant (CA), and why are they important?

To thrive as a Chartered Accountant, you need a strong background in accounting principles, financial analysis, and auditing, typically supported by a recognized CA or equivalent accounting certification. Expertise in accounting software such as SAP, QuickBooks, or Oracle, as well as proficiency in Excel and relevant tax systems, is often required. Attention to detail, analytical thinking, and integrity are crucial soft skills for ensuring accuracy and ethical financial reporting. These skills and qualifications are vital for maintaining regulatory compliance, supporting business decisions, and upholding stakeholder trust.

What are Clinical Research Associates (CRAs)?

Clinical Research Associates (CRAs) are professionals responsible for monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and good clinical practice guidelines. They act as a bridge between clinical trial sites and sponsors, overseeing the progress of studies, verifying data, and ensuring the safety and rights of participants. CRAs may travel frequently to different trial locations and play a crucial role in the successful execution of medical research.

How does a CRA (Clinical Research Associate) typically collaborate with site staff and sponsors during a clinical trial?

A CRA serves as a vital link between the clinical trial sponsor and the investigational site staff. They regularly communicate with site personnel to ensure compliance with study protocols, resolve issues, and verify data accuracy. CRAs also coordinate with sponsors by providing updates, reporting findings, and facilitating site visits. This collaboration helps maintain high-quality standards and ensures that trials progress smoothly and according to regulatory guidelines.

What is the difference between Cra vs Clinical Research Associate?

AspectCraClinical Research Associate
CredentialsTypically requires a degree in life sciences or related field; certifications like CCRP or RAC are commonSame as Cra, often holds certifications like CCRP or RAC
Work EnvironmentWorks on clinical trial sites or in offices, monitoring study progressMonitors clinical trials, manages site compliance, and ensures protocol adherence
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

The term Cra is often used interchangeably with Clinical Research Associate, as both roles involve monitoring clinical trials, ensuring compliance, and working within the same industry. The main difference is that Cra is a broader abbreviation, while Clinical Research Associate is the full job title. Both require similar credentials and work environments, making them essentially the same role described differently.

More about Cra jobs
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Cra jobs near you
Infographic showing various Cra job openings in the United States as of July 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 78% In-person, 11% Hybrid, and 11% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

CRA

Servier

Forest City, NC

Other

Posted yesterday

Job description

CRA

POSITION TITLE: CLINICAL RESEARCH ASSOCIATE (CRA)

REPORTS TO: Project Manager

 LOCATION: MADRID (SPAIN)

MISSION: Ensure that clinical trials are conducted, documented, and reported in full compliance with the study protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements. The purpose is to protect the rights, safety, and well-being of study participants while ensuring the quality, integrity, and reliability of the data collected.

REQUIREMENTS FOR THE POSITION :

 Experience

  • 3-4 years as CRA
  • At least 2 years Oncology experience
  • Extensive experience in monitoring oncologic patients across multiple clinical trials
  • Experience of monitoring of phase 2-3 and pivotal studies, Phase 1b is an add on
  • Able to manage complex design, including SIVs, monitoring during recruitment phase
  • Demonstrate by management of a substantial number of sites / subjects.
Skills:
  • Communication: strong interpersonal and negotiation skills with investigators and site staff
  • Problem-solving: Ability to identify and resolve protocol deviations or compliance issues
  • Organization: Strong attention to detail and ability to manage multiple sites/projects proactively
  • Time management skills: ability to work independently and manage multiple tasks effectively
  • Agility: demonstrate ability to adapt to new tools, processes and technologies in clinical researc
  • IInterest and capacity to learn new ways of working and increase scope of responsibilities to grow in the role
Languages
  • Spanish: business level
  • English: business slevel
Others: 
  • Driven licence

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