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Clinical Trial Research Assistant Jobs (NOW HIRING)

Baptist Health

Clinical Research Coordinator

Lexington, KY · On-site

$24 - $32/hr

The CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of ...

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Baptist Health

Clinical Research Coordinator

Lexington, KY · On-site

$24 - $32/hr

The CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of ...

Houston Methodist

$20.50 - $27.25/hr

Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...

Headlands Research

Research Assistant

Lake Worth, FL · On-site

$17 - $23.50/hr

As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... Clinical Research Assistant Location: Lake Worth, FL | Site Name: JEM Research Institute ...

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Clinical Trial Research Assistant information

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How much do clinical trial research assistant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trial research assistant in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What does a clinical trial research assistant do?

A Clinical Trial Research Assistant supports the organization and execution of clinical trials by handling tasks such as data collection, maintaining study documentation, scheduling participant visits, and ensuring compliance with regulatory guidelines. They work closely with clinical research coordinators and investigators to assist in the smooth running of clinical studies. Their responsibilities also include communicating with study participants, managing study supplies, and helping to prepare reports for regulatory agencies. This role is essential to the successful and ethical completion of clinical research projects.

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

To thrive as a Clinical Trial Research Assistant, you need a solid understanding of clinical research methods, attention to detail, and typically a bachelor's degree in life sciences or a related field. Familiarity with data management systems, electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, communication, and the ability to collaborate effectively with research teams set outstanding candidates apart. These competencies ensure accurate data collection, regulatory compliance, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial research assistants in managing study documentation?

Clinical Trial Research Assistants often encounter challenges in maintaining accurate and up-to-date study documentation, as regulatory requirements are strict and audits can occur unexpectedly. Balancing multiple studies or sites can make it difficult to keep protocols, consent forms, and data collection records organized. Attention to detail, strong time-management skills, and proficiency with electronic data capture systems are essential for overcoming these challenges and ensuring compliance with Good Clinical Practice (GCP) guidelines.

What is the difference between Clinical Trial Research Assistant vs Clinical Research Coordinator?

AspectClinical Trial Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRA are optionalRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient monitoring, and administrative tasks within clinical trial sitesManages study logistics, regulatory compliance, and patient recruitment at clinical sites or research institutions
Employer & IndustryHospitals, research institutions, pharmaceutical companiesResearch organizations, hospitals, pharmaceutical companies

The Clinical Trial Research Assistant primarily supports data collection and patient monitoring, while the Clinical Research Coordinator oversees study management and regulatory compliance. Both roles are essential in clinical research but differ in responsibilities and scope.

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Clinical Trial Research Assistant jobs near you
Infographic showing various Clinical Trial Research Assistant 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 $78,347 per year, or $37.7 per hour.

Clinical Trial Research Assistant

The Woodlands, TX • On-site

Advanced Rheumatology of Houston
Outpatient Health Care • 1 - 10 employees
Learn more about Advanced Rheumatology of Houstonexternal

$15 - $18/hr

Full-time

Re-posted 11 days ago

Job description

Clinical Trial Research Assistant
The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic/Onsite

Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. This is an exciting opportunity to be involved in cutting-edge medical research in a supportive and dynamic outpatient setting.

Key Responsibilities:
  • Process and ship biological specimens per study protocol.
  • Maintain lab inventory and order clinical trial supplies.
  • Ensure accurate and complete study documentation in compliance with institutional and federal regulations.
  • Support research coordinators with testing procedures and overall trial conduct.
  • Advertise, screen, recruit, and enroll patients in clinical trials.
  • Obtain informed consent and explain study participation clearly.
  • Schedule appointments, diagnostic tests, and study-related procedures.
  • Assist with data entry into electronic case report forms (eCRFs) and databases.
  • Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB).
  • Maintain knowledge of current study protocols and standard operating procedures.
  • Prepare for monitoring visits, sponsor audits, and regulatory inspections.
  • Help collect and report adverse events.
  • Attend ongoing training and continuing education relevant to research duties.

Preferred Skills:
  • Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
  • Experience with specimen processing, shipping, and documentation.
  • Bilingual (English/Spanish) is a plus.

Requirements:
  • Bachelor’s degree preferred; however, candidates with a strong work history and medical office experience will also be considered.
  • Previous lab experience with biological specimen handling.
  • Proficient in maintaining documentation and adhering to study protocols.
  • MUST live within 30 mins of The Woodlands.
  • THIS POSITION IS ONSITE.
  • Must be Technologically Adept.
  • Strong attention to detail and protocol compliance.
  • Excellent communication and organizational skills.

Why Join Us?
  • Supportive, collaborative team environment.
  • Opportunity to work on innovative, impactful clinical trials.
  • On-the-job training and professional development.
  • Regular weekday schedule with no night or weekend shifts.