Clinical Research Assistant: Data, Phlebotomy & Trials

Velocity Clinical Research, Inc.

Albuquerque (NM)

On-site

USD 38,000 - 52,000

Full time

4 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
PTO and company holidays
401(k) with company-match
Annual incentive program

Job summary

Velocity Clinical Research, Inc. is seeking a Clinical Research Assistant to support the Clinical Operations Team in collecting, documenting, and maintaining clinical data, including phlebotomy and administrative tasks.

You will assist with study conduct, data entry, specimen handling, and coordinating communications with sponsors and vendors, while upholding GCP standards and patient privacy requirements.

Qualifications

  • High School Diploma or technical degree with minimum 1 year of relevant experience in life sciences industry.
  • Demonstrated knowledge of medical terminology.
  • Demonstrated ability to multi-task and work as a team player.
  • Demonstrated ability to use computers and Microsoft Office software.

Responsibilities

  • Assist in conduct of clinical trials in accordance with study protocol, GCP, ICH Guidelines, and Velocity SOPs.
  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of protocol and local regulations.
  • Enter source data into sponsor/vendor data portal and resolve basic queries under supervision.
  • Maintain confidentiality of patient information and study records.
  • Prepare source documents and assist with front office duties as needed.

Skills

Medical terminology
Team player
Multi-tasking

Education

High School Diploma

Tools

MS Office
Computers

Job description

Velocity Clinical Research, Inc. is seeking a Clinical Research Assistant to support the Clinical Operations Team in collecting, documenting, and maintaining clinical data, including phlebotomy and administrative tasks.

You will assist with study conduct, data entry, specimen handling, and coordinating communications with sponsors and vendors, while upholding GCP standards and patient privacy requirements.

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