Clinical Research Assistant — Data & Phlebotomy Support

Velocity-Clinical-Research,-Inc.; Grand Island (NE); On-site; USD 40,000 - 52,000; Full time

Job summary

Velocity Clinical Research is seeking a Clinical Research Assistant to aid the Clinical Operations Team in data collection, documentation, and maintenance of clinical data, including phlebotomy and administrative duties. The role involves coordinating with sponsors, CROs, and vendors to ensure high-quality data and compliant trial processes.

The position supports patient care activities, source documentation, and regulatory documentation, with responsibilities spanning sample handling, data

Qualifications

• High School Graduate or technical degree with 1 year of life sciences experience.
• Phlebotomy certification if required by state law.
• Intramuscular dose administration and preparation if required by state law.
• Demonstrated knowledge of medical terminology.
• Proficiency with computers, Microsoft Office, fax, copier and multi-line phones.
• Ability to read, write and speak English.
• Ability to multi-task and work as a team.

Responsibilities

• Assist in conducting clinical trials per protocol, GCP, ICH and SOPs.
• Perform phlebotomy or other sample collection within protocol and regulatory requirements.
• Perform clinical assessments under supervision.
• Handle lab specimens, packaging, shipping per protocol or IATA regulations.
• Maintain inventory of lab and study supplies.
• Enter source data into sponsor/Vendor portals and resolve basic queries.
• Communicate with team, sponsors, CROs, and vendors.
• Understand and apply good documentation practices.

Skills

Medical terminology

MS Office

Team player

English proficiency

Multitasking

Written guidelines

Flexibility

Education

High School Graduate

Job description

Velocity Clinical Research is seeking a Clinical Research Assistant to aid the Clinical Operations Team in data collection, documentation, and maintenance of clinical data, including phlebotomy and administrative duties. The role involves coordinating with sponsors, CROs, and vendors to ensure high-quality data and compliant trial processes.

The position supports patient care activities, source documentation, and regulatory documentation, with responsibilities spanning sample handling, data