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Care Access · 1 day ago

Travel Clinical Research Assistant

United States

Full-time

Remote

Entry Level

$24/hr - $38/hr

1+ years exp

Care Access is dedicated to making the future of health better for all by providing world-class research and health services. The Travel Clinical Research Assistant will support clinical trials through various clinical and administrative tasks, with opportunities for growth within the organization.

Clinical TrialsHealth Care

No H1B

Responsibilities

Perform independent venipuncture; manage difficult draws and re-attempts per protocol

Collect, label, process, package, and ship biospecimens; maintain chain of custody and temperature controls

Set up/tear down event sites; prepare kits/supplies; uphold aseptic technique and biohazard safety

Communicate clearly with participants and on-site teams; escalate issues promptly

Ability to understand and follow institutional SOPs

Participate in recruitment and pre-screening events (may be multiple locations)

Assist with preparation of outreach materials

Request medical records of potential and current research participants

Schedule visits with participants, contact with reminders

Obtain informed consent per Care Access Research SOP, under the direction of the Clinical Research Coordinator (CRC)

Complete visit procedures as required by protocol, under the direction of the CRC

Record data legibly and enter in real time on paper or e-source documents

Request and issue study participant payments

Update all applicable internal trackers and online recruitment systems

Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc

Assist with maintaining all site logs

Assist with inventory and ordering equipment and supplies

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials

Maintain effective relationships with study participants and other Care Access Research personnel

Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management

Communicate clearly verbally and in writing

Perform other duties as assigned

Qualification

PhlebotomySpecimen processingClinical Practices (GCP)Medical terminologyMicrosoft Office SuiteCommunicationOrganizational skillsCritical thinkingTeam collaborationPositive attitude

Required

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

High level of self-motivation and energy

An optimistic, 'can do' attitude

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

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), CA/WA/LA/NV specific licensure/certification if role is based there