Clinical Research Assistant: Phlebotomy & Data Capture

Velocity Clinical Research, Inc.; Grand Island (NE); Hybrid; USD 42,000 - 54,000; Full time

Job summary

Velocity Clinical Research, Inc. seeks a Clinical Research Assistant to support the Clinical Operations Team in collecting, documenting, and maintaining clinical data, including phlebotomy and lab tasks. This role involves data entry, administrative duties, and collaboration with sponsors, CROs, and study personnel.

The position emphasizes accuracy, adherence to GCP/ICH guidelines, and safeguarding patient information while contributing to high-quality trial data and patient care.

Qualifications

• High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry.
• Phlebotomy certification may be required by state law.
• Demonstrated knowledge of medical terminology.
• Ability to use computers, MS Office, fax, copier, and multi-line phone.
• Strong organization, written and verbal communication skills.

Responsibilities

• Assist in conduct of clinical trials per protocol, GCP, ICH and SOPs.
• Perform venipuncture, capillary puncture and fluid collection as required.
• Under supervision, conduct clinical assessments (vital signs, ECG) within scope.
• Process, package and ship laboratory specimens per protocol and IATA rules.
• Maintain inventory of laboratory and study supplies and enter data into systems.

Skills

Medical terminology

Team player

English communication

Multi-tasking

Basic computer skills

Education

High School Diploma or Technical Degree

Tools

Microsoft Office

Data entry systems

Laboratory/medical equipment

Job description

Velocity Clinical Research, Inc. seeks a Clinical Research Assistant to support the Clinical Operations Team in collecting, documenting, and maintaining clinical data, including phlebotomy and lab tasks. This role involves data entry, administrative duties, and collaboration with sponsors, CROs, and study personnel.

The position emphasizes accuracy, adherence to GCP/ICH guidelines, and safeguarding patient information while contributing to high-quality trial data and patient care.