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Clinical Trial Research Associate Jobs (NOW HIRING)

Elixir Associates

Clinical Trial Manager

Santa Rosa, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

Sonoma, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

Hayward, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

San Mateo, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

San Jose, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

Mundelein, IL · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

Alameda, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

Elixir Associates

Clinical Trial Manager

Fremont, CA · On-site

Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like: Operational ownership of investigational sites. Study start-up ...

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As of Sep 11, 2026, the average hourly pay for clinical trial research associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

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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 10 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.