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Clinical Trials Research Associate information

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$36K

$94.3K

$143.5K

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

As of Sep 13, 2026, the average yearly pay for clinical trials research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 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 research—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 cities are hiring for Clinical Trials Research Associate jobs?

Cities with the most Clinical Trials Research Associate job openings:

What are the most commonly searched types of Clinical Trials Research jobs?

The most popular types of Clinical Trials Research jobs are:

What states have the most Clinical Trials Research Associate jobs?

States with the most job openings for Clinical Trials Research Associate jobs include:

What are popular job titles related to Clinical Trials Research Associate jobs?

For Clinical Trials Research Associate jobs, the most frequently searched job titles are:

Clinical Trials Research Associate jobs near you
Infographic showing various Clinical Trials Research Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Oncology Clinical Trials Nurse, Clinical Trials, FT, 8A-4:30P

Miami, FL • On-site

Baptist Health
Health Care and Social Assistance • 10K+ employees
Learn more about Baptist Healthexternal

$40.40 - $53.73/hr

Other

Re-posted 6 days ago

Baptist Health South Florida rating

8.1

Company rating: 8.1 out of 10

Based on 99 frontline employees who took The Breakroom Quiz

Job description

Oncology Clinical Trials Nurse

The Clinical Trials Nurse effectively conducts assigned operations of research protocols. Coordinates, evaluates and follows patient participation in clinical trials. Performs protocol specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses to the investigational treatment. Implement the standards for research protocols in compliance with regulatory, institutional and external agencies. Work within a Nurse-APRN-Physician ambulatory care model. Performs patient and family education / support. Collaborates with physicians in determining eligibility of patients for clinical trials. Acts as an expert consultant to investigators and others to ensure that Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOP's) are followed. Provides education to staff and patients on disease pathophysiology, treatment plans and clinical trial information. Identify patient problems and recommend plan of care. The estimated pay range for this position is $40.40 - $53.73 / hour depending on experience.

Degrees: Bachelors Degree is required. Licenses & Certifications: Basic Life Support. ACRP Certified Clinical Research Associate. SOCRA Certified Clinical Research Professional. Collab Inst Training Init. ONS/ONCC Chemotherapy Immunotherapy Certificate. Registered Nurse. Additional Qualifications: BSN-Bachelors degree in Nursing. RNs hired after 2/2012 with an Associate degree will have 5 years from their date of hire to complete the BSN degree. CITI must be obtained within the first 30 days of employment. ONS chemotherapy certificate must be obtained within first 6 months of employment, Association of Clinical Research Professional (ACRP) Certification or Certified Clinical Research Professional (CCRP) Certification within 1 year of employment. Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts. Experience with computer data entry and database management. Excellent written and oral communication skills. Excellent organizational skills. Attention to details and accuracy. Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents. Ability to work independently, organize, prioritize, and follow through with results. Ability to solve practical problems and implement solutions. Effective communicator, approachable and comfortable with diverse groups of people. Aware and abide by all standards that govern good clinical practices and general nursing practice. Years of Experience: A minimum of 1 year of experience is required.

Research

Miami

Baptist Health Herbert Wertheim Cancer Institute

Full-time

Ongoing EOE, including disability/vets

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About Baptist Health South Florida

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Baptist Health South Florida is the largest healthcare organization in the region, with 12 hospitals, more than 27,000 employees, 4,000 physicians and 100 outpatient centers, urgent care facilities and physician practices spanning across Miami-Dade, Monroe, Broward and Palm Beach counties. Baptist Health has internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences. A not-for-profit organization supported by philanthropy and committed to its faith-based charitable mission of medical excellence, Baptist Health has been recognized by Fortune as one of the 100 Best Companies to Work For in America and by Ethisphere as one of the World's Most Ethical Companies.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Miami, FL, US

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