Pediatric Oncology Clinical Research Coordinator II

Carilionclinic

Roanoke (VA)

In loco

USD 45.000 - 63.000

Tempo pieno

4 giorni fa
Candidati tra i primi

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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Comprehensive Medical, Dental, &Vision
Employer Funded Pension Plan (Vol. 403
Paid Time Off (accrued from day one)
Onsite fitness and wellness programs
Health/wellness app access

Descrizione del lavoro

Carilion Clinic seeks a Clinical Research Coordinator II in Pediatric Oncology in Roanoke, VA. You will coordinate studies, manage recruitment and consent, and ensure regulatory compliance throughout the research process.

You will collect and analyze data, maintain study documentation, and communicate with sponsors and IRBs while supporting monitoring visits and audits. A strong analytical mindset and organizational skills are essential.

Competenze

  • Bachelor's degree required or 4 years of experience may be considered in lieu of degree.
  • Minimum 2 years of healthcare or research experience required.
  • IATA certification required; research certification preferred.

Mansioni

  • Coordinates clinical research studies and ensures regulatory compliance.
  • Manages recruitment, screening, and enrollment of participants.
  • Obtains informed consent and handles study documentation.
  • Ensures adherence to study protocols and regulatory requirements.
  • Collects, manages, and analyzes study data.
  • Maintains study databases and regulatory documents.
  • Tracks adverse events and protocol deviations.
  • Communicates with sponsors, IRBs, and research teams.
  • Supports monitoring visits and audits.

Conoscenze

Analytical skills
Organizational skills
Communication

Formazione

Bachelor's degree or 4 years experience in lieu of degree

Descrizione del lavoro

Carilion Clinic seeks a Clinical Research Coordinator II in Pediatric Oncology in Roanoke, VA. You will coordinate studies, manage recruitment and consent, and ensure regulatory compliance throughout the research process.

You will collect and analyze data, maintain study documentation, and communicate with sponsors and IRBs while supporting monitoring visits and audits. A strong analytical mindset and organizational skills are essential.

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