Research Fellow Translational & Clinical Research

National Cancer Centre Singapore Pte Ltd; Singapore; On-site; SGD 90,000 - 120,000; Full time

Job summary

A leading oncology research organization seeks a Study Design Lead to advance lung cancer research across Asia. The role includes developing rigorous study designs for multi-country trials, collaborating with key stakeholders, and ensuring compliance with international standards. The ideal candidate has a Master’s or PhD in Life Sciences and at least 7 years of experience in clinical research with a proven track record in study design. This position is based in Singapore and offers an opportunity to impact patient outcomes significantly.

Qualifications

• Master’s or PhD required in a relevant field; MBBS/MD preferred.
• Minimum 7 years of experience in clinical research.
• At least 3 years in study design or medical affairs.

Responsibilities

• Lead development of study concepts and designs.
• Draft and refine study protocols and feasibility analyses.
• Serve as liaison between various stakeholders.

Skills

Scientific Writing & Communication

Analytical & Problem-Solving

Stakeholder Engagement

Organisational & Project Management

Regulatory & Compliance Awareness

Education

Master’s or PhD in Life Sciences, Pharmacy, Public Health, or related field

MBBS/MD

Tools

MS Office

Clinical Trial Management Systems (CTMS)

Job description

The Asian Thoracic Oncology Research Group (ATORG) is the coordinating platform for translational research in Asia. Its mission is to advance medical knowledge of lung cancer and improve health outcomes of patients through clinical studies and scientific events. ATORG operates under National Cancer Centre Singapore.

The Asia Pacific Oncology Drug Development Consortium (APODDC) was formed in 2020 as a platform to foster education and collaboration between key stakeholders of oncology drug development within the Asia Pacific region, thereby improving treatment access to patients. APODDC drives regional activities in collaboration with institutions in the region and industry partners.

ThisStudy Design Leadrole will lead the scientific and operational design of ATORG and APODDC’s multi-country oncology research programs, ensuring that all studies are scientifically rigorous, operationally feasible, and aligned with the consortium’s mission to deliver high-impact evidence that advances cancer care in the Asia-Pacific region.

Main Responsibilities:

1. Scientific Communication & Publication (30%)

• Lead development of study concepts, designs, and protocols for multi-country IITs and translational studies.
• Collaborate with PIs, scientific committees, and industry partners to define objectives, endpoints, and biomarker strategies.
• Ensure designs integrate translational science, statistical methodology, and regulatory requirements.
• Lead manuscripts and abstract development as well as coordinate conference presentation for ESMO Asia and WCLC

2. Protocol & Feasibility Development (25%)

• Draft and refine study protocols, synopses, schema, and feasibility questionnaires.
• Conduct feasibility assessments with participating sites, considering country-specific operational challenges.
• Integrate site capabilities, recruitment targets, and vendor requirements into study plans

3. Stakeholder Engagement (15%)

• Serve as liaison between ATORG/APODDC leadership, site investigators, CROs, and vendors.
• Facilitate consensus meetings, advisory boards, and protocol review committees.
• Engage with pharma, biotech, and funding bodies for study collaboration.

4. Quality Assurance (QA) Integration (15%)

• Embed quality-by-design principles into protocol and operational workflows.
• Review study-specific operational, safety monitoring, and data management plans for compliance with ICH-GCP and consortium SOPs.
• Ensure protocols and trial documents are audit-ready before finalisation.

5. Operational & Quality Oversight (10%)

• Collaborate with Clinical Operations to ensure designs are executable within timelines and budgets.
• Support the development of safety monitoring, QA frameworks, and data management plans.
• Ensure compliance with ICH-GCP, local regulations, and consortium SOPs.

6. Manage other tasks (5%)

• Contribute to grant applications, scientific publications, and conference presentations.
• Support training and mentoring of junior team members in study design and protocol development.
• Undertake other responsibilities as assigned by the PI.

Key Requirements:

• Master’s OR PhD in Life Sciences, Pharmacy, Public Health, or related field; MBBS/MD preferred.
• Formal training or certification in clinical research, medical writing, or biostatistics will be an advantage.
• Minimum 7 years’ experience in clinical research, with at least 3 years in study design, medical affairs, or scientific writing/publication roles.
• Proven track record in designing and implementing multi-country investigator-initiated trials or equivalent academic-led research.
• Experience integrating QA/quality-by-design principles into clinical study planning.
• Demonstrated success in developing and publishing peer-reviewed manuscripts and abstracts for scientific meetings.
• Prior experience working with multi-stakeholder research consortia, academic institutions, or industry collaborators in the Asia-Pacific region.

* Advantageous Skills to Have:

• Scientific Writing & Communication: Excellent ability to translate complex scientific and clinical data into clear, accurate protocols, manuscripts, and presentations.
• Analytical & Problem-Solving: Strong capability to evaluate scientific feasibility, identify risks, and propose practical solutions.
• Stakeholder Engagement: Skilled in managing relationships with investigators, sponsors, vendors, and internal teams across different cultures and geographies.
• Organisational & Project Management: Ability to manage multiple projects concurrently, meet deadlines, and maintain attention to detail.
• Regulatory & Compliance Awareness: Competence in ensuring study design, documentation, and publications comply with international and local regulations, SOPs, and ethical standards.
• Technical proficiency with MS Office, reference management software, and clinical trial management systems (CTMS) is desirable.