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Cra Training Jobs in Raleigh, NC (NOW HIRING)

410 ICR United States USA

Senior CRA

Cary, NC · On-site

Senior CRA Phase I Oncology NC ICON is a global healthcare intelligence and clinical research ... Providing training and guidance to site staff and other CRAs to maintain high standards of clinical ...

410 ICR United States USA

Senior CRA

Raleigh, NC

Sr CRA Phase 1 Oncology - Midwest ICON is a global healthcare intelligence and clinical research ... Providing training and guidance to site staff and other CRAs to maintain high standards of clinical ...

Icon plc

Senior CRA

Cary, NC · On-site

Senior CRA Phase I Oncology NC ICON is a global healthcare intelligence and clinical research ... Providing training and guidance to site staff and other CRAs to maintain high standards of clinical ...

Belcan

Clinical Research Associate 3

Durham, NC · On-site

$50.02 - $62.53/hr

The CRA is expected to apply strong clinical judgment in early-phase oncology settings, including ... training, enrollment oversight, and ongoing site engagement. * Track and follow critical site ...

Intellectt INC

Clinical Research Associate 3

Durham, NC · On-site

$50 - $62/hr

The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative ... training, enrollment oversight, and ongoing site engagement. * Track and follow critical site ...

Belcan

Clinical Research Associate 3

Durham, NC

$50.02 - $62.53/hr

The CRA is expected to apply strong clinical judgment in early-phase oncology settings, including ... training, enrollment oversight, and ongoing site engagement. * Track and follow critical site ...

5PY IQVIA RDS Inc.

Research Associate

Durham, NC

$47K - $169K/yr

Req • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Some organizations require completion of CRA training program or prior monitoring ...

5PY IQVIA RDS Inc.

Research Associate

Durham, NC

$47K - $169K/yr

Req • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Some organizations require completion of CRA training program or prior monitoring ...

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Showing results 21-40

All JobsCra Training JobsCra Training Jobs in Raleigh, NC

Cra Training information

See Raleigh, NC salary details

$10.7K

$77.2K

$133.7K

How much do cra training jobs pay per year?

As of Aug 6, 2026, the average yearly pay for cra training in Raleigh, NC is $77,219.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,100.00 and $132,700.00 per year, depending on experience, location, and employer.

What is the difference between Cra Training vs Clinical Research Associate?

AspectCra TrainingClinical Research Associate
Required CredentialsTraining programs, certifications (e.g., CCRP)Typically requires a degree in life sciences and certification
Work EnvironmentClassroom, online courses, training sessionsMonitoring sites, data review, site communication
Industry UsagePrepares individuals for clinical research rolesPerforms monitoring and oversight in clinical trials

Cra Training provides foundational education and certifications to prepare individuals for roles in clinical research. A Clinical Research Associate (CRA) is a professional who applies this training by monitoring clinical trials, ensuring compliance, and managing site activities. While Cra Training is focused on education, a CRA is an active role within the industry, often requiring prior training or certification.

What is CRA training?

CRA training refers to the education and preparation provided to individuals seeking to become Clinical Research Associates. This training covers topics such as Good Clinical Practice (GCP), clinical trial protocols, regulations, monitoring procedures, and ethical considerations. The goal is to equip trainees with the knowledge and skills needed to monitor clinical trials, ensure data integrity, and maintain compliance with regulatory standards. CRA training is essential for those entering the field of clinical research to ensure patient safety and accurate data collection.

What are some common challenges faced during CRA training and how can trainees overcome them?

During CRA training, one common challenge is mastering complex regulatory requirements and Good Clinical Practice (GCP) guidelines, which are essential for ensuring compliance in clinical trials. Trainees may also find it difficult to adapt to the fast-paced nature of clinical research and the need to manage multiple studies simultaneously. To overcome these obstacles, it's important to actively engage in hands-on learning, seek mentorship from experienced CRAs, and utilize available training resources such as workshops and online modules. Building strong organizational and communication skills early on will also help trainees succeed as they transition into independent monitoring roles.

How to become a certified CRA?

To become a certified Clinical Research Associate (CRA), candidates typically need a bachelor's degree in a health-related field and relevant experience in clinical research. Certification from organizations like the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA) is often required or preferred, which involves passing an exam and maintaining ongoing education. Developing skills in monitoring, regulatory compliance, and data management is also important for certification and career advancement.

What qualifications do I need to be a CRA?

To become a Clinical Research Associate (CRA), candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP) guidelines, and strong organizational skills are also important; some roles may require certification such as the RAC or CCRP.

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, knowledge of Good Clinical Practice (GCP) guidelines, and often a bachelor's degree in a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and relevant certifications such as ACRP or SOCRA are typically required. Strong attention to detail, organizational skills, and effective communication help CRAs manage multiple studies and collaborate with sites. These skills ensure regulatory compliance, data integrity, and smooth coordination of clinical trials.
What are popular job titles related to Cra Training jobs in Raleigh, NC? For Cra Training jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Cra Training jobs in Raleigh, NC look for? The top searched job categories for Cra Training jobs in Raleigh, NC are:
Cra Training jobs near you
Infographic showing various Cra Training job openings in Raleigh, NC as of July 2026, with employment types broken down into 9% Locum Tenens, 76% Full Time, 5% Part Time, 1% Contract, and 9% Summer. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $77,219 per year, or $37.1 per hour.

Senior CRA

410 ICR United States USA

Cary, NC • On-site

Full-time

Posted 12 days ago

Job description

Senior CRA Phase I Oncology NC

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply