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Clinical Trials Research Associate Jobs in Raleigh, NC

Sr Clinical Research Associate

Raleigh, NC Β· On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to ... The Sr. CRA will participate in the planning, development, and execution of clinical trials to ...

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Clinical Trials Research Associate information

See Raleigh, NC salary details

$35K

$91.7K

$139.5K

How much do clinical trials research associate jobs pay per year?

As of Sep 14, 2026, the average yearly pay for clinical trials research associate in Raleigh, NC is $91,676.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,800.00 and $124,400.00 per year, depending on experience, location, and employer.

What does a clinical trials research associate do?

A Clinical Trials Research Associate (CRA) is responsible for monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with protocols, regulatory requirements, and good clinical practice guidelines. CRAs often act as the main line of communication between clinical trial sites and the sponsoring company. Their duties include site selection, training site staff, verifying data accuracy, and ensuring patient safety. They play a crucial role in the development of new drugs and medical devices by ensuring the integrity and quality of clinical research data.

What skills and qualifications are needed to be a clinical trials research associate?

To thrive as a Clinical Trials Research Associate, you need a solid background in life sciences, knowledge of clinical research methodologies, and often a degree in a related field. Familiarity with regulatory guidelines (such as GCP), clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly required. Excellent organizational skills, attention to detail, and strong communication abilities help you collaborate effectively with study teams and ensure accurate documentation. These competencies are crucial for maintaining compliance, data integrity, and the overall success of clinical research projects.

What challenges do clinical trials research associates face when coordinating multiple studies?

Clinical Trials Research Associates often juggle several studies at once, which requires exceptional organizational and time-management skills. One common challenge is ensuring each study complies with regulatory standards and timelines, while also maintaining accurate documentation across all projects. Balancing communication between investigators, sponsors, and regulatory bodies can also be demanding, but strong collaboration and proactive problem-solving help manage these complexities. Staying adaptable and detail-oriented is key to successfully overseeing multiple trials.

What is the difference between Clinical Trials Research Associate vs Clinical Data Coordinator?

AspectClinical Trials Research AssociateClinical Data Coordinator
CredentialsBachelor's degree in life sciences or related field; often requires clinical research certificationsBachelor's degree in health sciences, biology, or related; may also hold clinical research certifications
Work EnvironmentClinical trial sites, hospitals, research organizationsData management departments, clinical research offices
Employer & IndustryPharmaceutical companies, CROs, academic institutionsPharmaceutical companies, CROs, healthcare organizations
Search & Comparison IntentOften compared for roles in clinical trial management and site coordinationCompared for roles focusing on data accuracy and database management

The Clinical Trials Research Associate primarily oversees trial conduct at sites, ensuring protocol adherence, while the Clinical Data Coordinator manages and verifies trial data. Both roles require similar educational backgrounds and certifications, but they focus on different aspects of clinical researchβ€”site management versus data management.

How hard is it to get a clinical trials research associate job?

Securing a clinical trials research associate position typically requires a relevant bachelor's degree in health sciences, biology, or a related field, along with some experience or training in clinical research. Competition can be moderate, and having certifications like the Certified Clinical Research Professional (CCRP) can improve job prospects. Strong organizational skills and familiarity with regulatory guidelines are also important for success in this role.

How much does a clinical trials research associate get paid?

A clinical trials research associate typically earns between $50,000 and $70,000 annually, depending on experience, location, and the complexity of trials. Entry-level positions may start lower, while experienced associates or those with specialized skills can earn higher salaries. Compensation often includes benefits such as health insurance and paid time off.

Is a clinical trials research associate a good career?

A clinical trials research associate (CRA) is a valuable role in the healthcare and pharmaceutical industries, responsible for monitoring and managing clinical trial processes to ensure compliance and data integrity. The position offers opportunities for career growth, requires attention to detail, and often involves collaboration with medical professionals and regulatory agencies. It typically requires a background in life sciences and may benefit from certifications such as SOCRA or ACRP.

What are the most commonly searched types of Clinical Trials Research jobs in Raleigh, NC?

The most popular types of Clinical Trials Research jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Trials Research Associate jobs?

Cities near Raleigh, NC with the most Clinical Trials Research Associate job openings:

Infographic showing various Clinical Trials Research Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $91,676 per year, or $44.1 per hour.

Senior Clinical Research Associate - Oncology

Durham, NC β€’ On-site

Worldwide Clinical Trials
Scientific Research and Development ServicesΒ β€’Β 10K+ employees

Full-time

Posted 7 days ago


Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!

What you will do

  • Responsible for managing the research activities at sites participating in Worldwide's clinical research projects

  • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded

  • Conduct study initiation visits (SIVs)

  • While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Superior organizational skills with attention to detail

  • Ability to work with little or no supervision

  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

  • 5+ years of experience as a Clinical Research Associate

  • 4-year universitydegree OR Nursing Degree

  • Experience in Oncology is required

  • Candidates must reside in the United States

  • Willingness to travel regionally required

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $0.00 - $1,000,000.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.