Clinical Research Coordinator, Neonatology (Contract)

KK WOMEN'S AND CHILDREN'S HOSPITAL PTE. LTD.

Singapore, Singapore
Ich-gcp and protocol compliance
Source document preparation
Sae and susar reporting
The role involves independently administering clinical trials in accordance with ICH-GCP and specific protocol requirements

Job Summary

  • The role involves independently administering clinical trials in accordance with ICH-GCP and specific protocol requirements.
  • Candidates must ensure full accountability of study equipment and investigational products while managing subject-related issues.
  • The position requires preparing source documents, handling data queries, and assisting with CIRB and HSA submissions.

Matching Summary

Match Score: 85

The role involves independently administering clinical trials in accordance with ICH-GCP and specific protocol requirements.

Skills & Requirements

Must-have

  • ICH-GCP and protocol compliance
  • Source document preparation
  • SAE and SUSAR reporting
  • Investigator site file maintenance
  • CIRB and HSA submission assistance

Nice-to-have

  • Strong communication skills
  • People-management skill
  • Team-player attitude
  • Intermediate computer skills
  • Budget monitoring experience

Key Requirements

  • Degree/Diploma in Life Sciences/Pharmacy/Nursing
  • Minimum 6 years CRC or relevant experience
  • Demonstrated competency in clinical research

Work Rights

Not specified

Tailored Resume

Cover Letter