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Education & Training 🏢 Full Time ⭐️ Terverifikasi

Senior Executive/Assistant Manager (Study Monitor)

National University of Singapore
National University Of Singapore, Central Region
Estimasi Gaji
SGD 4.500 – SGD 7.500
Live Update
9 Juli 2026
Batas Akhir
9 Jul 2027

Deskripsi Pekerjaan

The National University of Singapore (NUS) is seeking a highly organized and detail-oriented professional to join our dynamic team as a Senior Executive/Assistant Manager (Study Monitor). In this pivotal role, you will be responsible for overseeing the integrity, compliance, and operational efficiency of research studies and clinical trials conducted within our academic environment.

As a Study Monitor, you will play a critical role in bridging the gap between project protocols and field execution. You will ensure that all data collection processes adhere to Good Clinical Practice (GCP) guidelines, institutional policies, and regulatory requirements. This is an excellent opportunity for an experienced professional looking to make a significant impact in a world-class educational and research institution, working alongside leading academics and researchers to push the boundaries of innovation.

Tanggung Jawab

  • Monitor research study activities to ensure strict compliance with institutional protocols and regulatory guidelines.
  • Conduct regular site visits and audits to verify the accuracy of data collection and record-keeping.
  • Coordinate with principal investigators and research teams to resolve discrepancies or non-compliance issues promptly.
  • Prepare comprehensive monitoring reports, detailing study progress, issues identified, and corrective actions taken.
  • Assist in the training of research staff on updated study protocols and documentation requirements.
  • Ensure the safety and confidentiality of participant data in accordance with PDPA and institutional privacy standards.
  • Maintain effective communication channels with internal and external stakeholders to facilitate smooth project operations.

Kualifikasi

  • Bachelor’s degree in Life Sciences, Healthcare, Research Administration, or a related field.
  • Minimum 3-5 years of experience in clinical trial monitoring, quality assurance, or research operations.
  • Strong working knowledge of Good Clinical Practice (GCP) and research regulatory frameworks.
  • Exceptional analytical skills with the ability to interpret complex protocols and data sets.
  • Proficiency in Microsoft Office Suite and specialized research data management software.
  • Strong interpersonal and communication skills, with the ability to engage effectively with stakeholders at all levels.
  • Ability to work independently, manage tight deadlines, and handle multiple priorities simultaneously.

Keahlian yang Dibutuhkan

Clinical Research Study Monitoring Regulatory Compliance Data Quality Assurance SOP Development Stakeholder Management Project Management Good Clinical Practice (GCP)

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