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Project Manager (PTSMDT)

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Onsite

Project Manager (PTSMDT)

NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD

Project Manager (PTSMDT)

Skills

Data ScienceMachine LearningAICompliance

18 days ago

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Important information


Location:

Singapore

Work mode:

Onsite

Published on:

6 October 2026

What they need


Job Category: Research

Posting Date: 6 Oct 2026

We are seeking a highly motivated and entrepreneurial Project Manager to support the Platform for Translational Systems Medicine (PTSM), a SingHealth-Duke NUS joint initiative co-led by Prof Enrico Petretto, Prof Salvatore Albani, and Prof Daniel Tan, and related initiatives within the Clinical Trials and Epidemiological Sciences (CTE) Programme and Duke-NUS collaborations.

The successful candidate will play a key role in coordinating translational research programmes, evaluating novel therapeutic and diagnostic assets, and supporting the development and execution of investigator-initiated clinical trials (IITs), particularly early-phase studies.

This role requires a strong understanding of data science, translational medicine, immunology, clinical research, and regulatory considerations, with the ability to bridge scientific, clinical, operational, and industry stakeholders.

Key Responsibilities:

1.Programme and Project Management

  • Lead and coordinate activities across the PTSM programme and associated translational research initiatives.
  • Track project milestones, deliverables, budgets, timelines, and reporting requirements.
  • Facilitate communication among clinicians, scientists, bioinformaticians, industry partners, and institutional stakeholders.
  • Develop project plans and ensure timely execution of programme objectives.
  • Work closely with the core PTSM team, including the Project Manager and Programme Manager, to drive the progression of SingHealth therapeutic, diagnostic, and digital health assets towards key translational milestones and value inflection points.

2.Translational Research and Scientific Evaluation

  • Support the evaluation and prioritisation of novel therapeutic, diagnostic, and digital health assets.
  • Conduct scientific, competitive landscape, and translational assessments of emerging opportunities.
  • Work closely with researchers to identify pathways for clinical translation and commercial development.

3.Clinical Trial Development and Support

  • Assist in the design, planning, and implementation of investigator-initiated trials (IITs), early-phase clinical studies, and retrospective and prospective validation cohort studies.
  • Coordinate protocol development, feasibility assessments, study start-up, and operational planning.
  • Liaise with clinical research units, sponsors, and external collaborators to ensure smooth study execution.
  • Monitor study progress and support issue resolution across multiple stakeholders.

4.Regulatory and Governance Support

  • Provide project oversight for regulatory submissions and approvals.
  • Coordinate interactions with ethics committees, institutional review boards, regulatory agencies, and research administration offices.
  • Ensure compliance with institutional, national, and sponsor requirements.
  • Support contract, funding, and governance processes related to translational research projects.

5.Strategic Partnerships

  • Engage academic, healthcare, industry, and funding partners to develop collaborative opportunities.
  • Identify and evaluate new funding, partnership, and translational opportunities.
  • Contribute to strategic planning and programme growth initiatives.
  • Work with academic, healthcare, and industry partners to evaluate and advance novel therapeutic, diagnostic, and digital health technologies towards clinical and commercial translation.

Key Requirements:

  • Minimum Bachelor’s degree in Life Sciences, Biomedical Sciences, Immunology, Data Science, Public Health, or related discipline.
  • Experience in translational research, biomedical innovation, clinical research, or programme management.
  • Strong understanding of clinical trial development and conduct.
  • Familiarity with regulatory and ethical requirements governing clinical research.
  • Excellent project management, communication, and stakeholder engagement skills.
  • Ability to work effectively across multidisciplinary teams.
  • Experience supporting investigator-initiated trials (IITs) and early-phase clinical studies.
  • Knowledge of oncology, immunology, precision medicine, or systems biology.
  • Understanding of bioinformatics, AI, machine learning, or healthcare data science applications.
  • Experience working with academic-industry partnerships or translational funding programmes.
  • Exposure to technology evaluation, due diligence, innovation management, or commercialisation activities.

Req ID: 5183

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