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Jobs or company...

Clinical Monitoring / Clinical Trial Consultant (1~3 year project)

  • Full Time, onsite
  • Redbock - an NES Fircroft company
  • Kawasan Sekitar Kuala Lumpur, Malaysia
Salary undisclosed

Apply on

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We are seeking a Clinical Monitoring/ CT Consultant on behalf of a world-leading medical device manufacturer. This role will oversee and ensure the quality and compliance of clinical trials in Malaysia.

Potential Start Date: October through February

Contract Length: Minimum 12 months, up to 3 years

Work Schedule: Part-time (0.5 FTE) and full-time (1 FTE) options available

Work Arrangement: 3 days in the office (Kuala Lumpur), 2 days working from home

Reports To: Head of Clinical Research, APAC

Key Responsibilities:

  • Conduct site visits to ensure compliance with protocols, GCP, and regulations; monitor patient safety; and manage adverse event reporting.
  • Verify clinical trial data accuracy, guide sites for protocol adherence, and review CRFs to resolve discrepancies.
  • Collaborate with ethics committees, regulatory bodies, and internal teams; maintain clear communication; and engage with key opinion leaders and advisory boards.

Qualifications:

  • Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
  • 3~7 years of experience in clinical monitoring or a related role, preferably in a Medical Device organization
  • Strong knowledge of GCP, regulatory requirements, and clinical trial processes.
  • Excellent organizational and communication skills.
  • Fluency in English and Bahasa Malaysia
  • Willingness to travel as required.

How to Apply: Please send your resume to [email protected].

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