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Clinical Research Analyst Jobs (NOW HIRING)

Innovo Research

Clinical Research Coordinator

Hutchinson, KS · On-site

$21 - $28/hr

JOB SUMMARY A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and ... Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and ...

RWJBarnabas Health

Research Coordinator

Livingston, NJ · On-site

$35 - $40/hr

Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

RWJBarnabas Health

Research Coordinator

Livingston, NJ · On-site

$35 - $40/hr

Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

RWJBarnabas Health

Research Coordinator

Livingston, NJ · On-site

$35 - $40/hr

Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

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Clinical Research Analyst information

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$38.5K

$74K

$99.5K

How much do clinical research analyst jobs pay per year?

As of Sep 10, 2026, the average yearly pay for clinical research analyst in the United States is $73,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What is a clinical research analyst?

A Clinical Research Analyst is a professional who specializes in collecting, analyzing, and interpreting data from clinical trials and medical studies. They play a crucial role in ensuring the accuracy and integrity of research data, which helps guide healthcare decisions and regulatory approvals. Their responsibilities may include designing data collection systems, monitoring study progress, and preparing reports for stakeholders. Clinical Research Analysts often work in hospitals, pharmaceutical companies, or research organizations, collaborating with scientists, doctors, and regulatory agencies.

What are the key skills and qualifications needed to thrive as a clinical research analyst?

To thrive as a Clinical Research Analyst, you need a solid background in life sciences or healthcare, strong analytical skills, and familiarity with clinical research methodologies, often supported by a relevant degree. Proficiency with data analysis tools such as SAS, SPSS, or R, and knowledge of regulatory systems like FDA or ICH-GCP guidelines, are typically required. Attention to detail, effective communication, and problem-solving abilities are vital soft skills for managing complex data and collaborating with research teams. These skills and qualities ensure accurate data interpretation, regulatory compliance, and successful execution of clinical studies.

What types of teams and departments do clinical research analysts typically collaborate with during a clinical trial?

Clinical Research Analysts often work cross-functionally with various teams, including clinical operations, regulatory affairs, data management, and biostatistics. They coordinate closely with principal investigators, study coordinators, and sometimes external partners like contract research organizations. This collaboration ensures that data collection, reporting, and regulatory submissions are accurate and timely. Being able to communicate effectively across disciplines is essential for success in this role.

What is the difference between Clinical Research Analyst vs Clinical Data Coordinator?

AspectClinical Research AnalystClinical Data Coordinator
Required CredentialsBachelor's degree in life sciences, certifications like CCRP or RAC often preferredBachelor's degree in health sciences, certifications like CDMP or CCRC beneficial
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Employer & Industry UsageUsed in clinical research, pharmaceutical, biotech industriesCommon in clinical trial management and data handling
Comparison Search IntentUnderstanding roles, responsibilities, and qualificationsFocus on data management and coordination tasks

The Clinical Research Analyst and Clinical Data Coordinator roles share similarities in their focus on clinical trials and data handling, but differ mainly in responsibilities. The analyst interprets data and supports research analysis, while the coordinator manages data collection and entry. Both roles require relevant degrees and certifications, and are vital in the clinical research industry.

Do you need a degree to be a clinical research analyst?

A clinical research analyst typically needs at least a bachelor's degree in a related field such as life sciences, healthcare, or statistics. Some positions may require additional certifications or experience with data analysis tools and clinical trial processes. Educational background and relevant skills are important for entry and advancement in this role.

Is clinical research in high demand?

Clinical research analysts are in high demand due to the ongoing need for new medical treatments and advancements in healthcare. The field offers growth opportunities, especially for those with strong analytical skills, knowledge of regulatory requirements, and experience with data management tools. Employment is expected to grow faster than average in the coming years.
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Clinical Research Analyst jobs near you
Infographic showing various Clinical Research Analyst 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 $73,965 per year, or $35.6 per hour.

Clinical Research Coordinator Auburn AL

Auburn, AL • On-site

Medovation Clinical Research LLC
See more jobs at Medovation Clinical Research LLCexternal

$22 - $28/hr

Part-time

Medical, Dental, PTO

Posted 21 days ago

Key responsibilities

  • Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.

  • Analyze data collected during trials and maintain accurate records for compliance management.

  • Oversee blood sampling procedures and ensure proper handling and documentation.

Job description

Benefits
Competitive salary
Dental insurance
Health insurance
Paid time off
Training & development
About Us
We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role.
Role Overview
Here's an opportunity to work for a dynamic and growing clinical research company. We have a fantastic and supportive work environment. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies. This position works on-site at the physician’s practice. This position requires a detail-oriented individual with a strong background in medical terminology, data management, and clinical trials management. The ideal candidate will have at least two (2) years of experience coordinating all aspects of clinical research projects from initiation to completion. Phlebotomy skills required. 
Key Responsibilities
Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
Analyze data collected during trials and maintain accurate records for compliance management.
Oversee blood sampling procedures and ensure proper handling and documentation.
Train on clinical trial protocols and procedures.
Collaborate with healthcare professionals to ensure participant safety and integrity of data.
Utilize software for data capture and reporting
Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders.
Ensure compliance with ethical standards and regulatory requirements throughout the research process.
Required Qualifications
Clinical experience preferred but not required
Experience in Sleep Clinical Trails preferred
Experience in clinical trials 2+ years of coordinator experience
Proficiency in data entry
Knowledge of medical terminology relevant to clinical research.
Phlebotomy and blood sampling techniques is required
Patient Recruitment experience required
Excellent organizational skills with attention to detail and the ability to manage multiple tasks simultaneously
What We Offer
A mission-driven and collaborative team culture.
Opportunities for career growth as the company scales.
The chance to contribute meaningfully to expanding access to clinical research for underserved populations.
If you’re looking for an opportunity to take ownership, build something from the ground up, and make a significant impact, we’d love to hear from you!
Compensation: $22.00 - $28.00 per hour
Medovation Clinical Research is an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. We value impactful work, open collaboration, and a spirit of diversity and inclusion.