Clinical Trials Project Specialist (End-to-End Study Management) #HDC

RECRUIT EXPRESS PTE LTD

Singapore
Lead clinical study planning and execution
Manage protocols and informed consent materials
Perform site qualification and monitoring visits
This role offers the opportunity to work alongside cross-functional teams to drive the successful delivery of clinical trials from planning through execution

Job Summary

  • This role offers the opportunity to work alongside cross-functional teams to drive the successful delivery of clinical trials from planning through execution.
  • Key responsibilities include developing essential study documents, liaising with investigative sites, and performing clinical monitoring activities such as initiation and close-out visits.
  • The position requires ensuring accurate reporting of adverse events and protocol deviations while maintaining strict compliance with Good Clinical Practice guidelines.

Matching Summary

Match Score: 85

This role offers the opportunity to work alongside cross-functional teams to drive the successful delivery of clinical trials from planning through execution.

Skills & Requirements

Must-have

  • Lead clinical study planning and execution
  • Manage protocols and informed consent materials
  • Perform site qualification and monitoring visits
  • Ensure GCP compliance and regulatory adherence
  • Collaborate with CROs and external vendors

Nice-to-have

  • Strong analytical capabilities for data interpretation
  • Experience preparing clinical reports and publications
  • Ability to present at investigator meetings
  • Cross-functional team collaboration skills
  • Database oversight experience

Key Requirements

  • Degree in Science, Life Sciences, Public Health, Pharmacy, Medicine, or Nursing
  • Familiarity with Good Clinical Practice (GCP) guidelines
  • Strong attention to detail and organizational capabilities

Work Rights

Not specified

Tailored Resume

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