Senior Executive/Assistant Manager (Study Monitor)

NATIONAL UNIVERSITY OF SINGAPORE

Singapore, Singapore
Not specified
Conduct qualification and initiation visits
Ensure protocol adherence and gcp compliance
Monitor clinical study site progress and data
The National University of Singapore is seeking a Senior Executive/Assistant Manager to serve as a Study Monitor within the ADVANcing Clinical Evidence in Infectious Diseases Network. The role involves overseeing clinical study sites to ensure compliance with protocols and regulatory requirements, with a focus on improving public health through better management of drug-resistant infections

Job Summary

  • The role involves performing study monitoring for the ADVANCE ID network focused on drug-resistant infections.
  • Candidates must supervise clinical sites to ensure adherence to protocols, regulatory requirements, and subject safety.
  • The position requires developing recruitment strategies while maintaining strict compliance with SOPs and Good Clinical Practice.

Matching Summary

Match Score: 85

The National University of Singapore is seeking a Senior Executive/Assistant Manager to serve as a Study Monitor within the ADVANcing Clinical Evidence in Infectious Diseases Network. The role involves overseeing clinical study sites to ensure compliance with protocols and regulatory requirements, with a focus on improving public health through better management of drug-resistant infections.

Skills & Requirements

Must-have

  • Conduct qualification and initiation visits
  • Ensure protocol adherence and GCP compliance
  • Monitor clinical study site progress and data
  • Evaluate investigational product management
  • Develop patient recruitment strategies

Nice-to-have

  • Experience in matrixed team environments
  • Ability to work with limited oversight
  • Strong interpersonal communication skills
  • Self-driven capacity with sense of urgency

Key Requirements

  • Site Management or equivalent experience in clinical research
  • BSc or MSc in relevant field
  • Understanding of clinical trials methodology and terminology
  • Proficiency with EDC, eTMF, and CTMS systems

Work Rights

Not specified

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