Oncology Research Assistant: Grant-Funded Data & Compliance

CP01 Carilion Medical Center

Roanoke (VA)

On-site

USD 21,000 - 29,000

Full time

14 days+
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Benefits offered by this job

Comprehensive Medical, Dental, &Vision
Employer Funded Pension Plan
Paid Time Off
Onsite fitness and wellness programs
Education and training opportunities

Job summary

Carilion Clinic in Roanoke, VA is seeking a Clinical Research Assistant to support oncology studies, including industry sponsored and grant funded research, ensuring compliance with guidelines and institutional policy. You will assist with data collection, document submission, consent development, and coordination of monitoring visits, while maintaining study logs and communicating with sponsors and IRBs.

Bachelor’s degree required; IATA certification; strong computer, organizational and

Qualifications

  • Bachelor's degree in science or related field required; 4 years of clinical research experience may be considered in lieu of degree.
  • IATA certification is required.
  • Excellent computer skills and strong organizational and communication abilities.

Responsibilities

  • Assists with administrative activities for research studies including industry sponsored and grant funded.
  • Supports completion and submission of study related documentation and develops and maintains study logs.
  • Coordinates with study team, sponsors, CROs, IRB, and other departments to ensure smooth protocol implementation and ongoing maintenance.
  • Monitors enrollment, develops informed consent materials, schedules visits, and maintains data collection from multiple sources.

Skills

Computer skills
Organizational skills
Communication skills

Education

Bachelor's degree in science

Tools

IATA certification

Job description

Carilion Clinic in Roanoke, VA is seeking a Clinical Research Assistant to support oncology studies, including industry sponsored and grant funded research, ensuring compliance with guidelines and institutional policy. You will assist with data collection, document submission, consent development, and coordination of monitoring visits, while maintaining study logs and communicating with sponsors and IRBs.

Bachelor’s degree required; IATA certification; strong computer, organizational and

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