Clinical Research Coordinator II — Grants & Trials

ChristianaCare

Belgique

Sur place

EUR 25 000 - 38 000

Plein temps

Il y a 12 jours

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Avantages offerts par ce poste

Full medical, dental, vision, life ins
403(b) with company contributions
Paid time off with roll-over
12-week paid parental leave

Résumé du poste

ChristianaCare is seeking a Research Coordinator to provide administrative and operational support for research projects in both outpatient and inpatient settings. You will coordinate NICHD Federal grants and other sponsored clinical trials, ensuring study procedures, data collection, and regulatory compliance are followed.

Under supervision, you will liaise with Principal Investigators, sponsors, and staff; manage study documentation and shipments, and support monitoring visits and audits.

Qualifications

  • Minimum of a high school diploma or equivalent required.
  • Associate degree in related science preferred but not required.
  • Minimum of two years of clinical or research experience required.
  • OB/GYN experience is a plus.
  • Fluent in Spanish a plus.
  • Phlebotomy skills preferred.

Responsabilités

  • Coordinate study-related activities from start-up through completion.
  • Ensure adherence to GCP Guidelines and SOPs.
  • Screen, recruit, schedule, consent, and conduct study visits.
  • Collect and record data; monitor adverse events.
  • Maintain regulatory documentation and IRB submissions.
  • Order and stock study supplies; coordinate shipment of specimens.

Formation

High school diploma
Associate degree in related science

Outils

REDCap
Medrio
OpenClinica

Description du poste

ChristianaCare is seeking a Research Coordinator to provide administrative and operational support for research projects in both outpatient and inpatient settings. You will coordinate NICHD Federal grants and other sponsored clinical trials, ensuring study procedures, data collection, and regulatory compliance are followed.

Under supervision, you will liaise with Principal Investigators, sponsors, and staff; manage study documentation and shipments, and support monitoring visits and audits.

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