Clinical Trial Research Assistant at Advanced Rheumatology of Houston
The Woodlands, TX 77382, USA -
Full Time


Start Date

Immediate

Expiry Date

11 Sep, 25

Salary

18.0

Posted On

11 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Phlebotomy, Documentation, Shipping

Industry

Pharmaceuticals

Description

CLINICAL TRIAL RESEARCH ASSISTANT

The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic
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.

PREFERRED SKILLS:

  • Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
  • Strong attention to detail and protocol compliance.
  • Excellent communication and organizational skills.Experience with specimen processing, shipping, and documentation.
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REQUIREMENTS:

  • Bachelor’s degree or higher in a science-related field* US University * (e.g., biology, chemistry, biochemistry).
  • Previous lab experience with biological specimen handling.
  • Proficient in maintaining documentation and adhering to study protocols.
  • Bilingual (English/Spanish) is a plus.MUSTV live within 30 mins of The Woodlands.
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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.
  • 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.
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