Sign upLog in

Clinical Trial Research Assistant

Advanced Rheumatology of Houston

The Woodlands, Texas

Apply
JOB DETAILS
SALARY
$15–$18
SKILLS
Adverse Events, Biochemistry, Biological Processes, Biology, Calendar Management, Case Report Form (CRF), Chemistry, Clinical Assessment, Clinical Research, Clinical Trial, Communication Skills, Data Entry, Detail Oriented, Documentation, Electrocardiogram, English Language, FDA (Food and Drug Administration), Federal Laws and Regulations, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Inventory Management, Laboratory, Medical Products, Medical Research, Multilingual, Order Supplies, Organizational Skills, Outpatient Care, Phlebotomy, Regulations, Regulatory Reports, Research Protocols, Sample/Specimen Processing, Shipping Documents, Spanish Language, Standard Operating Procedures (SOP), Team Player, Testing
LOCATION
The Woodlands, Texas
POSTED
30+ days ago
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 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.
  • 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.

About the Company

A

Advanced Rheumatology of Houston