Carilion Clinic

Carilion Clinic

Clinical Research Coordinator IV - Oncology

Roanoke, Virginia · Full-time

Sponsorship not specified$63k-$95kDetected 21 days ago
AuditingClinical TrialsClinical ResearchFDA RegulatoryResearchLeadershipCommunicationMentoring

About the role

  • Serves as liaison between research sponsors, site management organizations, local Institutional Review Board (IRB), physicians/staff, and R&D.
  • Assists in writing research grant proposals, manuscripts, study materials, brochures, and correspondence. - Acts as a champion for clinical research at Carilion Clinic.
  • Knowledge of medical and/or pharmaceutical terminology strongly desired.

Responsibilities

  • Carilion understands the importance of prioritizing your well-being to help you develop and thrive.

Requirements

  • strong knowledge of word processing, spreadsheets, databases, and internet environment.
  • Strong organization and communication skills required.
  • Must have strong leadership, interpersonal and teamwork skills.
  • Nationally recognized clinical research certification from Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) required upon hire.
  • I.A.T.A. (International Air Transport Association) certification is required for projects that will be transporting specimens prior to completion of IRB application.
  • Bachelor's degree in science or related field required.

Nice to have

  • Master's degree in science or related field preferred.

Skills

  • Recruit, screen, and enroll eligible study participants.
  • Obtain informed consent from study participants.
  • Manages completion and submission of study related documentation.
  • Collects data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
  • Collect, process, and ship research specimens as directed in the protocol.
  • Ensure compliance with study protocol and requirements of regulatory agencies.
  • Tracks and reports adverse events and protocol deviations.
  • Coordinates all site related monitoring or auditing visits from sponsor or federal agency during the course of the study and at closure.
  • Demonstrates competency managing multiple complex studies and significant workload.
  • Provides in-depth clinical research training and mentorship to junior and intermediate CRCs.
  • Contributes to trial planning, development, and implementation activities.
  • Assists with protocol feasibility determination, identifying potential barriers and proactively solving problems.

Compensation

  • $63,377.60 - $95,076.80 Employee pay is based on a variety of factors, including qualifications, credentials, education, and prior work experience.
  • The compensation range does not include benefits or pension plan.
  • RHONDA JOHNSON Recruiter Email:
  • rejohnson@carilionclinic.org
  • For more information, contact the HR Service Center at 1-800-599-2537.
  • Carilion is a Drug-Free Workplace.

Benefits

  • Comprehensive Medical, Dental, & Vision Benefits
  • Employer Funded Pension Plan, vested after five years (Voluntary 403B)
  • Paid Time Off (accrued from day one)
  • Access to our health and wellness app, Personify Health
  • Continued education and training
  • Benefits, Pay and Well-being at Carilion Clinic
  • That's why we offer a well-rounded benefits package, and many perks and well-being resources to help you live a happy, healthy life - at work and when you're away.
  • Below are benefits available to you when you join Carilion:
  • Onsite fitness studios and discounts to our Carilion Wellness centers

Equal opportunity

  • We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age (40 or older), disability, genetic information, or veterans status.
  • Carilion is a Drug-Free Workplace.
  • For more information or for individuals with disabilities needing special assistance with our online application process contact Carilion HR Service Center at 800-599-2537, 8:00 a.m. to 4:30 p.m., Monday through Friday.

Visa & Work Authorization

  • Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance

This listing is sourced directly from Carilion Clinic's careers page and normalized into a canonical job model.