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Entry Level Clinical Research Assistant Jobs (NOW HIRING)

M3USA

Clinical Research Assistant

Chattanooga, TN

The Clinical Research Assistant (RA) supports the daily execution of clinical trial activities under the guidance of site leadership, the Principal Investigator (PI), and the clinical research staff.

M3USA

Clinical Research Assistant

Chattanooga, TN · On-site

The Clinical Research Assistant (RA) supports the daily execution of clinical trial activities under the guidance of site leadership, the Principal Investigator (PI), and the clinical research staff.

Massgeneralbrigham

Clinical Research Assistant

Belmont, MA · On-site

$21.53 - $29.08/hr

The Clinical Research Assistant will be primarily responsible for recruitment and follow-up of participants in two studies that recruit across multiple hospital-based inpatient units within McLean ...

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Entry Level Clinical Research Assistant information

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How much do entry level clinical research assistant jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for entry level clinical research assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What is an Entry Level Clinical Research Assistant job?

An Entry Level Clinical Research Assistant supports clinical trials by assisting with data collection, documentation, and ensuring compliance with study protocols. They help coordinate participant visits, maintain study records, and communicate with research teams. This role provides hands-on experience in clinical research and is ideal for those looking to start a career in healthcare or pharmaceuticals. Strong attention to detail and organizational skills are essential for success.

What does a typical day look like for an Entry Level Clinical Research Assistant?

As an Entry Level Clinical Research Assistant, your day often involves supporting the study team by collecting and entering data, organizing study documents, scheduling participant visits, and assisting with regulatory paperwork. You may help prepare materials for clinical trials, ensure adherence to study protocols, and communicate with participants or site staff to address questions or coordinate schedules. Collaboration with clinical coordinators, investigators, and sometimes laboratory staff is a regular part of the job. This variety keeps each day dynamic and offers great opportunities to learn about the research process while developing essential industry skills.

What are the key skills and qualifications needed to thrive in the Entry Level Clinical Research Assistant position, and why are they important?

To thrive as an Entry Level Clinical Research Assistant, you typically need a bachelor's degree in a life science or related field, attention to detail, strong organizational skills, and basic knowledge of clinical research protocols. Familiarity with electronic data capture systems, Microsoft Office Suite, and understanding of Good Clinical Practice (GCP) guidelines are often required or preferred. Strong communication, teamwork, and problem-solving abilities help you build effective relationships with research teams and study participants. These skills ensure accurate data collection, compliance with regulatory standards, and smooth coordination of clinical trials.

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Entry Level Clinical Research Assistant jobs near you
Infographic showing various Entry Level Clinical Research Assistant job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 70% Full Time, 23% Part Time, 1% Temporary, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.
Travel Clinical Research Assistant

Travel Clinical Research Assistant

Care Access

San Antonio, TX • On-site

$24 - $38/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 14 hours ago

Job description

How This Role Makes A Difference
The Travel Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization. 
 
This role will perform a variety of clinical and administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.Much of the work for this role will be done onsite at a clinical event or site location. 
How You'll Make An Impact
  • Perform independent venipuncture; manage difficult draws and re-attempts per protocol. 
  • Collect, label, process, package, and ship biospecimens; maintain chain of custody and temperature controls. 
  • Set up/tear down event sites; prepare kits/supplies; uphold aseptic technique and biohazard safety. 
  • Communicate clearly with participants and on-site teams; escalate issues promptly. 
  • Ability to understand and follow institutional SOPs.  
  • Participate in recruitment and pre-screening events (may be multiple locations). 
  • Assist with preparation of outreach materials. 
  • Request medical records of potential and current research participants. 
  • Schedule visits with participants, contact with reminders. 
  • Obtain informed consent per Care Access Research SOP, under the direction of the Clinical Research Coordinator (CRC). 
  • Complete visit procedures as required by protocol, under the direction of the CRC. 
  • Record data legibly and enter in real time on paper or e-source documents.  
  • Request and issue study participant payments. 
  • Update all applicable internal trackers and online recruitment systems. 
  • Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.   
  • Assist with maintaining all site logs.  
  • Assist with inventory and ordering equipment and supplies.  
  • Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. 
  • Maintain effective relationships with study participants and other Ccare Access Research personnel. 
  • Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management. 
  • Communicate clearly verbally and in writing. 
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. 
The Expertise Required
  • Bilingual proficiency required: Must be fluent in both English and Spanish, with the ability to effectively communicate (written and verbal) in both languages.
  • Ability and willingness to work independently with minimal supervision. 
  • Ability to learn to work in a fast-paced environment. 
  • Excellent communication skills and a high degree of professionalism with all types of people 
  • Excellent organizational skills with strong attention to detail 
  • A working knowledge of medical and research terminology 
  • A working knowledge of federal regulations, Good Clinical Practices (GCP) 
  • Critical thinker and problem solver 
  • Friendly, outgoing personality with the ability to maintain a positive attitude under pressure. 
  • Contribute to team and site goals. 
  • Proficiency in Microsoft Office Suite 
  • High level of self-motivation and energy 
  • An optimistic, "can do" attitude. 
Certifications/Licenses, Education, and Experience:
  • 1+ year recent hands-on phlebotomy experience in a clinical setting. 
  • 200 total venipunctures; 25-50 capillary sticks; 30-50 sticks in the last 2-3 months. 
  • Some Clinical Research experience preferred. 
  • Demonstrated competency in specimen processing. 
  • Working knowledge of ICH-GCP, basic research terminology, and HIPAA/PHI handling. 
  • Comfortable using mobile apps/eSource and standard office tools. 
  • Current national phlebotomy certification (one of): 
  • ASCP Phlebotomy Technician (PBT) 
  • AMT Registered Phlebotomy Technician (RPT) 
  • NHA Certified Phlebotomy Technician (CPT) 
  • NCCT National Certified Phlebotomy Technician (NCPT) 
  • CA/WA/LA/NV specific licensure/certification if role is based there 
How We Work Together
  • Location: Candidates must be willing to travel in support of community events within your metropolitan area and occasional national travel.
  • Travel: Duties may require travel in the following models: 
    • Tuesday through Saturday Work Weeks 
    • Temporary Event Support (3-7-day deployment durations) 
    • Frequency and length of travel may depend on the length and location of study, site, and event. 
    • Deployments normalize to a 32 to 42-hour work week on average.
    • Must possess a valid driver's license and be able to operate rental vehicles provided for work-related travel. 

The expected salary range for this role is $24.00 - $38.00 USD per hour for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match 

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