Travel Clinical Research Assistant
Care Access•Humble, TX
•$24 - $38•Onsite
About The Position
The Travel Clinical Research Assistant is an entry-level role that provides clinical and administrative support for research studies while offering hands-on training and professional development within clinical research. Working primarily at clinical sites and community events, this position assists with study operations, participant interactions, and data collection, contributing to the successful execution of clinical trials. The role offers opportunities for growth and advancement within the organization.
Requirements
- 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
- 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)
- Must possess and maintain a valid Driver’s License (Valid / Authorized to Drive in Canada and the US)
- Must have and maintain safe driving record and submit to Motor Vehicle Record Check
- A minimum of 1-year recent phlebotomy experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
- Phlebotomy experience and proficiency required.
- ~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
- 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.
Nice To Haves
- Some Clinical Research experience preferred.
Responsibilities
- Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant relationships throughout the research process.
- Perform venipuncture, collect, process, package, and ship biospecimens, maintain specimen integrity and chain of custody, and adhere to infection control, safety, and protocol requirements.
- Accurately document study activities in real time, maintain study logs and trackers, request medical records and participant payments, and ensure compliance with FDA regulations, ICH-GCP, study protocols, and Care Access SOPs.
- Prepare clinical event sites and supplies, manage inventory, support outreach activities, perform administrative tasks, and collaborate effectively with research staff and external stakeholders.
Benefits
- 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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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
