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Clinical Research Analyst Jobs (NOW HIRING)

Sr. Clinical Research Coordinator

Manhattan, NY · On-site

$26.75 - $35.50/hr

Clinical Research Analyst Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and ...

Sr. Clinical Research Coordinator

Manhattan, NY · On-site

$26.75 - $35.50/hr

Clinical Research Analyst Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and ...

... Research Analyst role for our company. We are based in India and USA and this position will be ... various clinical research related tasks and requirements. Some understanding of basic medical ...

Research Analyst

Lexington, KY · On-site

$17.76 - $28.43/hr

Posting Details Job Title Research Analyst Requisition Number RE55648 Working Title Department Name ... Responsibilities include participant recruitment and screening, clinical research data collection ...

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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 9, 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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What states have the most Clinical Research Analyst jobs?

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What are popular job titles related to Clinical Research Analyst jobs?

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

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 Analyst I - Clinical Research Hub

Gainesville, FL • On-site

University of Florida
Colleges, Universities, and Professional Schools • 5 - 10K employees

$53K - $60K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


University Of Florida rating

7.2

Company rating: 7.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

391st of 633 rated colleges and universities


Job description

Clinical Research Analyst I - Clinical Research Hub
Job no: 541172
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Grant or Research Administration, Health Care Administration/Support
Department:29011701 - MD-OR CLINICAL RESEARCH HUB
Classification Title:
Clinical Research Analyst I
Classification Minimum Requirements:
Bachelor's degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
Job Description:
Are you passionate about clinical research and looking for an opportunity to make a meaningful impact? The University of Florida's Clinical Research Hub is seeking a Clinical Research Analyst I to join our team and support impactful clinical research initiatives.
The Clinical Research Analyst will be a member of the Clinical Trials Support Office within the University of Florida's (UF) Clinical Research Hub (CRH). The Analyst will be responsible for assisting in building protocols in UF's Clinical Trials Management System (CTMS) for the Academic Health Center's (AHC) and the Oncology (ONC) human subject clinical research projects under the purview of CRH. The Analyst is expected to assist with the protocols, provide quality checks, and implement institutional guidelines and procedures.
The team member is expected to work collaboratively with other members, as well as study teams. The professional knowledge and expertise required includes but is not limited to proficiency in the CTMS or similar research software, proficiency in Microsoft Office (Excel, Word, and Outlook), general knowledge of Clinical Trials. The Analyst is responsible for assisting with task list timelines assigned within UF's CTMS.
MORE ABOUT THIS POSITION:
INTAKE AND ASSESSMENTS
  • Responsible for completing project intake submission assessments, assisting with research billing grid reviews, and finalizing associated documentation
  • Review multiple documents related to research projects to ensure adherence to institutional guidelines
  • Review Cost Language Template selections for informed consent forms

PORTFOLIO MANAGEMENT
  • Responsible for managing assigned portfolio, maintaining protocol records, building billing grids, and managing CRH workflows within the CTMS and being a navigator with Advarra
  • Gain proficiency in the CTMS to complete tasks, adjust records and assist UF research units regarding their use of the CTMS
  • Manage assigned portfolio, maintain protocol records, and oversee CRH workflows within the CTMS
  • Assist in protocol mitigation or corrections as needed

CUSTOMER SUPPORT AND END USER TRAINING
  • Acts as a liaison between Principal Investigator (PI), administrators, agency officials
  • Interacts closely with PI and their respective staff to provide technical assistance during the development process of clinical research budgets and agreements
  • Provides guidance to departmental staff, investigators, and research administrators on both sponsor-specific policy and UF requirements

CALENDAR SUPPORT and BUDGET BUILD SUPPORT
  • Build sponsor pays all AHC protocol calendars and budgets within the CTMS application
  • Works to submit, answer queries, and provide quality assurance and feedback for all calendars and budgets built by the vendor
  • Communicates with study teams, fiscal teams, and coverage analysis staff to ensure accuracy of each calendar
  • Makes edits as necessary throughout the calendar and budget development process

COVERAGE ANALYSIS SUPPORT
  • Work on assisting with protocol coverage analyses within the CTMS application and manage requests in a timely and professional manner
  • Complete Medicare Coverage Analysis (MCA) reviews with other team members
  • For MCAs acquired from the CTMS vendor, assist team members with validation and completion of the MCA(s) to ensure that they adhere to UF coverage analysis standards

We Offer Exceptional Benefits:
  • Low-cost State Health Plans: Medical, Dental, and Vision Insurance
  • Life and Disability Insurance
  • Generous Retirement Options to secure your future
  • Comprehensive Paid Time Off Packages with 10+ paid holidays, paid family, sick and vacation leave
  • Exceptional Personal and Professional Development Opportunities: Access to UF Training & Organizational Development programs, leadership development, LinkedIn Learning, and more
  • Tuition Assistance through the UF Employee Education Program
  • Public Service Loan Forgiveness (PSLF) Eligible Employer

Learn more about what we have to offer here!
About Gainesville, Florida:
Home to the University of Florida, one of the nation's top public universities, Gainesville offers vibrant academic and healthcare communities alongside an affordable cost of living, no state income tax, and mild winters. Enjoy the outdoors with over 30 miles of bike trails, freshwater springs, and numerous water activities, plus easy access to beaches and world-class theme parks.
Gainesville combines historic charm with modern amenities, including a great school system, a lively downtown, and a thriving local culture with farmers' markets and craft breweries. Discover professional growth and quality of life in Gainesville-where community, innovation, and work-life balance meet!
Expected Salary:
$53,000 - $60,000 annually; commensurate with education and experience.
Required Qualifications:
Bachelor's degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
Preferred:
The ideal candidate will possess:
  • One year of experience in business administration and/or financial management in an professional setting
  • Familiarity with the OnCore CTMS by Advarra or similar clinical trial management software
  • Ability to balance customer service and research compliance
  • Ability to organize and work effectively, prioritize, be flexible, and stay on task in a high-paced, high-volume professional environment
  • Skilled in problem solving techniques, critical thinking and creativity
  • Strong time management, organizational, documentation, attention to detail, and task follow up skills
  • Experience using Microsoft Office Applications

Special Instructions to Applicants:
To be considered, please upload the following:
  • Cover Letter
  • Resume
  • Contact information for three professional references

Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:No
Advertised: 31 Aug 2026 Eastern Daylight Time
Applications close: 14 Sep 2026 Eastern Daylight Time
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About University of Florida

Sourced by ZipRecruiter

The University of Florida is one of the top ranked public universities in the United States (ranked top 5 amongst public universities in 2023 US news and world report). It is one of only a few comprehensive universities, having medical, veterinary, dental, nursing, public health, and engineering disciplines all co-localized on the same, contiguous campus to facilitate interdisciplinary collaboration. Gainesville is located in the northern region of Florida, within 1-1.5 hours of each coast, and just 1.5-2 hours to Orlando and Tampa. It is a small to medium-sized city with a low cost of living, excellent public and private schools, and southern hospitality. While Gainesville is widely recognized as the home of the Gators, it is quickly becoming known as a center for innovation and a place with a lifestyle that's comfortable for families, yet attractive for young professionals.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Gainesville, FL, US

Year founded

1853