Clinical Research Coordinator (CRC)

Responsibilities

• Coordinate day-to-day site trial operations.
• Support patient recruitment, consent and retention.
• Maintain accurate source documents and eCRFs.
• Liaise between investigators, sponsors and CRAs.

Requirements

• Graduate in Life Sciences, Nursing or Pharmacy.
• 2+ years coordinating clinical trials.
• Familiarity with EDC systems and ICH-GCP.
• Strong organizational and communication skills.