Preclinical Programme Leader, Cardiovascular & Metabolic Diseases

A*STAR Research; Singapore; On-site; SGD 100,000 - 150,000; Full time

Benefits offered by this job

Attractive benefits

Long-term career growth opportunities

Job summary

A leading biomedical research institute in Singapore is seeking a Preclinical Programme Leader for Cardiovascular & Metabolic Diseases. This role will encompass overseeing siRNA and ASO development from target validation to candidate selection for clinical studies. The ideal candidate will have extensive experience in RNA therapeutics, strong hands-on laboratory skills, and a PhD in Molecular Biology or a related field. The position offers competitive compensation and opportunities for growth within Singapore's thriving biomedical ecosystem.

Qualifications

• Minimum of 4+ years (Scientist), 8+ (Senior Scientist) or 12+ (Principal Scientist) years of experience leading siRNA/ASO discovery programmes.
• Strong expertise in obesity and MASH disease models.
• Experience in early drug discovery from target validation to lead generation.

Responsibilities

• Own end-to-end scientific and project strategy for siRNA/ASO discovery programmes.
• Establish integrated workflows to support pipeline projects.
• Design and oversee in vivo PK/PD studies.

Skills

Hands-on laboratory expertise

Programme management skills

Collaborative mentoring

Data-driven leadership

Education

PhD in Molecular Biology, Pharmacology, Biochemistry or related discipline

Tools

In vivo PK/PD models

Cell-based assays

Job description

Job Description

Job Title: Preclinical Programme Leader, Cardiovascular & Metabolic Diseases

Requisition ID: 1659

Posting Start Date: 10/04/2026

The Nucleic Acid Therapeutics Initiative (NATi), hosted by A*STAR, is Singapore's national platform dedicated to advancing RNA-based medicines and revolutionising drug and vaccine development. NATi's mission is to establish Singapore as a globally recognised hub of excellence in nucleic acid therapeutics research, clinical translation, and commercialisation.

NATi focuses on key RNA modalities such as antisense oligonucleotides (ASOs), small interfering RNA (siRNA), and messenger RNA (mRNA). To drive this vision, NATi is building a biotech‑like translational engine focused on asset and technology development spanning discovery to clinical development.

We are actively seeking passionate and committed individuals with deep translational expertise to join us in advancing the next generation of RNA‑based therapeutics.

Position Overview

We are seeking a scientific Preclinical Programme Leader, Cardiovascular & Metabolic Diseases for discovery toward clinical development of oligonucleotide (siRNA/ASO) programmes targeting MASH, obesity, and cardiometabolic diseases. This role will own programmes from target validation to selection of a Preclinical Candidate ready for IND‑enabling studies.

The successful candidate will rely on hands‑on laboratory experience to establish discovery and preclinical development capabilities (e.g. in vitro models, animal models, PK/PD workflows) through a combination of internal build‑up and oversight of external CROs. The candidate will combine deep oligonucleotide modality expertise with programme management experience, and strategic oversight of the programme execution plan within budget and on time. The role will progress from hands‑on execution to building and mentoring a team to support multiple pipeline programmes.

Key Responsibilities

• Own end‑to‑end scientific and project strategy for one or more siRNA/ASO discovery programmes from target validation to selection of a Preclinical Candidate in MASH, obesity and/or musculoskeletal diseases.
• Establish and execute integrated in vitro and in vivo workflows to support pipeline projects and generate robust high‑quality data to support decision‑making process.
• Drive clear go/no‑go recommendations based on integrated assessment of biology, PK/PD, and disease‑relevant efficacy endpoints.
• Ensure scientific rigour, reproducibility, documentation, and transparency across internal and CRO‑executed activities.
• Actively contribute hands‑on laboratory operations as needed to establish platforms, assays, and workflows.

Oligonucleotide Discovery & Screening

• Design, execute, and optimise in vitro screening cascades for siRNA/ASO programmes across key metabolic tissues (liver, muscle, adipose), incorporating potency, durability, concentration response curve, and delivery‑dependent activity.
• Develop and deploy mechanistic and functional cell‑based assays to link target knockdown with metabolic pathway modulation and disease‑relevant phenotypes.
• Support discovery and optimisation of novel siRNA/ASO delivery platforms, with emphasis on enabling effective extrahepatic cellular uptake and functional knockdown.
• Lead hit identification, prioritisation, and lead generation by integrating in vitro potency, functional relevance, delivery compatibility, and translational hypotheses.
• Establish assay transferability and performance standards for internal execution and CRO deployment.
• Target Output: Enable rapid identification of lead siRNA/ASO candidates with validated tissue‑specific potency, functional relevance, delivery feasibility, and clear translational readiness for in vivo progression.

Pharmacology & Translation

• Design, oversee, and interpret in vivo PK/PD, biodistribution, and knockdown efficacy studies.
• Establish exposure‑response and knockdown‑response relationships to guide lead optimisation and selection.
• Select, justify, and govern disease‑relevant in vivo models for:
• MASH: histology, non‑invasive fibrosis and inflammation biomarkers.
• Obesity: metabolic, cardiometabolic, and weight‑related outcomes.
• Skeletal muscle: functional, metabolic, and mitochondrial readouts.
• Target Output: Deliver robust in vivo PK/PD and efficacy datasets linking exposure, knockdown, and disease‑relevant outcomes across MASH, obesity, and skeletal muscle models.

Disease Biology Expertise

• Deep expertise in liver biology, including:
  • MASH pathophysiology.
  • Hepatic lipid metabolism, inflammation, and fibrogenesis.
  • Translational biomarkers relevant to clinical development.
• Strong understanding of obesity biology, including:
  • Energy balance and metabolic regulation.
  • Adipose tissue inflammation, remodelling, and endocrine signalling.
• Working knowledge of skeletal muscle metabolism, insulin sensitivity, and glucose utilisation.
• Target Output: Apply deep, systems‑level disease biology expertise to guide target selection, target validation, in vitro and in vivo model selection to drive the pharmacology and biomarker strategy across liver, adipose, and skeletal muscle in metabolic disease.

Scientific Governance, Project Leadership & Collaboration

• Establish, author, and maintain SOPs for:
  • In vitro screening.
  • In vivo PK/PD and efficacy models.
  • Tissue distribution and early tolerability workflows.
• Lead or support IACUC/local animal ethics submissions, umbrella protocols, and regulatory compliance.
• Build, mentor, and manage junior scientists as programmes and internal capabilities scale.
• Act as primary scientific and operational interface with CROs, ensuring experimental quality, timelines, data integrity, and budget alignment.
• Serve as the biology/pharmacology point‑of‑contact with chemistry, bioinformatics, pathology, analytical, and external partners.
• Partner closely with senior management to align programme execution with portfolio strategy, resourcing, and milestone delivery.
• Target Output: Standardised, compliant biology‑pharmacology execution delivering high‑quality, reproducible data on time and within budget. Aligned teams and partners advancing programmes efficiently against portfolio milestones.

Qualifications & Professional Attributes

• PhD in Molecular Biology, Pharmacology, Biochemistry, or related discipline.
• A minimum of 4+ (Scientist), 8+ (Senior Scientist), 12+ (Principal Scientist) years of industry experience leading siRNA/ASO discovery programmes, ideally in CVMD.
• Strong hands‑on expertise in:
  • Cell‑based screening and mechanistic assays.
  • In vivo PK/PD and knockdown biology.
  • Obesity and MASH disease models.
• Demonstrated success in early drug discovery, from target validation through hit identification and lead generation.
• Experience establishing new capabilities or platforms and scaling programmes through CRO partnerships.
• Strong programme management skills with the ability to drive decision‑grade outcomes.
• Scientifically rigorous, data‑driven leader with excellent written and verbal communication skills.
• Collaborative mentor capable of balancing hands‑on execution, team building, and strategic ownership.

Global Recruitment & Competitive Compensation

NATi is conducting a global search for top‑tier talent in RNA therapeutics. We welcome applications from leading pharmaceuticals scientists and biotech innovators worldwide.

This role provides a highly competitive compensation package aligned with global industry standards, including attractive benefits and long‑term career growth opportunities within Singapore's thriving biomedical innovation ecosystem. Join us in shaping the future of RNA‑based medicines and establishing Singapore as a world‑class hub for nucleic acid therapeutics.

The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.