784 Medical Project jobs in Singapore

We are currently seeking clinicians to fill a Medical Research Doctor role.
You will work with our Global team of research and clinical professionals to facilitate the translation of research data and quality improvement programs into clinical practice and improvement of patient care. The role includes assisting with drafting and reviewing documentation and publications, project coordination and liaison with project teams, as well as presentation to external stakeholders and conference participation.
This is a fantastic opportunity to become involved in medical management and quality improvement projects with an internationally recognised research organisation.
This role offers home-based working from Singapore or hybrid working from our offices in Cambridge and Norwich, UK, on a full or part-time basis, with flexible working hours that can fit alongside caring arrangements or other clinical/research commitments.
Primary Responsibilities
To contribute to medical quality improvement programs.
To continually assess the benefit of our quality improvement programs to patients, and tailor the programs to maximise their real-life application in a clinical setting.
Review and contribute to scientific documents and publications (including proposals and reports).
To independently develop ethics applications for projects.
To contribute to new and existing projects with respect to considering practical medical issues and clinical application; and to understand EMR data and coding systems and give guidance on the application of data to projects.
Review and complete presentations, abstracts, and posters.
Communication and liaison with internal teams across various global locations.
Liaison with study sponsors and steering committee experts.
Presentations and calls with external stakeholders.
Participation and presentations at international medical/scientific conferences.
Qualifications
Doctor of medicine.
Minimum of 3 years of clinical experience ideally gained within the UK.
Clinical experience or scientific study in the field of respiratory medicine is an advantage.
Experience and Key Skills
UK clinical experience is preferred, ideally within NHS Primary Care.
An interest in research and scientific studies.
Experience in scientific writing, publication of peer-review journal publications is preferred.
Client relations, liaising with external parties internationally, strong leadership and presentation skills.
Excellent written and verbal English communication skills.
Salary
is dependent on experience.
Contact Us
Please send your CV with a covering letter summarising your suitability for the role to All candidates will be required to undertake a remote skills test prior to interview. We look forward to hearing from you.
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We are seeking a highly skilled and detail-oriented Project Coordinator to support our growing portfolio of medical interior projects. As a key member of our team, you will be responsible for coordinating and monitoring daily project activities, timelines, and deliverables.

• Coordinate and monitor daily project activities, timelines, and deliverables.
• Liaise with clients, consultants, subcontractors, and suppliers to ensure smooth project flow.
• Assist the Project Manager in preparing work schedules, shop drawings, method statements, and submissions.
• Track and update progress claims, VO, and defect rectifications.
• Manage document control, procurement tracking, and material follow-up.
• Attend site meetings and inspections, ensuring alignment between site works and documentation.
• Ensure compliance with MOM, SCDF, MOH, and other authority submissions.

• Diploma or Degree in Building, Construction, Architecture, or related field.
• 2–4 years of experience in interior fit-out or A&A projects (healthcare experience a bonus).
• Familiar with project documentation, AutoCAD/SketchUp/Bluebeam, and Microsoft Office.
• Good written and verbal communication skills.
• Proactive, independent, and a team player.
• Able to work under pressure and meet tight deadlines.

We offer a dynamic and supportive work environment, opportunities for professional growth and development, and a competitive compensation package.

Leveraging a diverse suite of platforms, Hilleman can rapidly respond to emerging needs to provide the right solution to control the impact of infections. Find out how we use these platforms in our R&D and manufacturing hub in Singapore

Targeted use of microbial species such as E. coli and P. pastoris as high productivity expression platforms, with a view to reducing cost of production.

Deploying cost-effective platforms for the production of various types of vaccines such as live-virus vector, attenuated, and inactivated vaccines.

Development of potential targets using the vesicular stomatitis virus (VSV) and measles virus vectors (MeV), both of which are established as stable and highly reliable platforms.

Using circular RNA as a vaccine modality could potentially offer greater biostability, thermostability and better immune responses with longer protective responses.

Leveraging polysaccharide conjugation to develop more effective vaccines which may be a safer alternative.

Leveraging a diverse suite of platforms, Hilleman can rapidly respond to emerging needs to provide the right solution to control the impact of infections. Find out how we use these platforms in our R&D and manufacturing hub in Singapore
Microbial
Targeted use of microbial species such as E. coli and P. pastoris as high productivity expression platforms, with a view to reducing cost of production.
Deploying cost-effective platforms for the production of various types of vaccines such as live-virus vector, attenuated, and inactivated vaccines.
Live Viral Vectors
Development of potential targets using the vesicular stomatitis virus (VSV) and measles virus vectors (MeV), both of which are established as stable and highly reliable platforms.
RNA-based Platform
Using circular RNA as a vaccine modality could potentially offer greater biostability, thermostability and better immune responses with longer protective responses.
Leveraging polysaccharide conjugation to develop more effective vaccines which may be a safer alternative.
#J-18808-Ljbffr

Hilleman Laboratories operates a first-of-its-kind vaccine development hub in Singapore, consisting of a research and development (R&D) facility at Biopolis, alongside a 30,000 square foot pilot-scale manufacturing facility at 138 Depot Road. The hub provides end-to-end product development solutions from concept to pilot manufacturing and Phase II clinical studies, supporting the development of affordable, high-value vaccines and biologics for low- and middle-income countries.

The state-of-the-art R&D facility in Biopolis undertakes process development, analytical development, drug product development and formulation for vaccines and biologics. It focuses on product development of vaccines and biologics, including candidate selection, design, early manufacturing process development and preclinical studies.

As one of the facilities of the dual-feature set up, the Good Manufacturing Practices (GMP) facility is capable of producing clinical trial material (up to Phase II) and is equipped with drug product fill-&-finish capability. This unique set-up enables the two facilities working in tandem to provide end-to-end product development, leveraging innovative technology platforms to develop affordable, high-value vaccines and biologics. The facility has also been designed to easily pivot to manufacture vaccines for emergency use during pandemics.

Hilleman is a critical connector, bringing together health ecosystem stakeholders for vaccines and biologics R&D and manufacturing. We collaborate with local, regional and global partners and stakeholders, including policymakers and governments, to facilitate wider, affordable access to life-saving vaccines and biologics. Apart from conducting translational research and product development, we also act as a catalyst for advancements in the biopharma industry by facilitating technology transfers, and capability building through manpower development initiatives.

Hilleman Laboratories operates a first-of-its-kind vaccine development hub in Singapore, consisting of a research and development (R&D) facility at Biopolis, alongside a 30,000 square foot pilot-scale manufacturing facility at 138 Depot Road. The hub provides end-to-end product development solutions from concept to pilot manufacturing and Phase II clinical studies, supporting the development of affordable, high-value vaccines and biologics for low- and middle-income countries.

Research and Development

The state-of-the-art R&D facility in Biopolis undertakes process development, analytical development, drug product development and formulation for vaccines and biologics. It focuses on product development of vaccines and biologics, including candidate selection, design, early manufacturing process development and preclinical studies.

GMP Pilot Manufacturing

As one of the facilities of the dual-feature set up, the Good Manufacturing Practices (GMP) facility is capable of producing clinical trial material (up to Phase II) and is equipped with drug product fill-&-finish capability. This unique set-up enables the two facilities working in tandem to provide end-to-end product development, leveraging innovative technology platforms to develop affordable, high-value vaccines and biologics. The facility has also been designed to easily pivot to manufacture vaccines for emergency use during pandemics.

Partnerships

Hilleman is a critical connector, bringing together health ecosystem stakeholders for vaccines and biologics R&D and manufacturing. We collaborate with local, regional and global partners and stakeholders, including policymakers and governments, to facilitate wider, affordable access to life-saving vaccines and biologics. Apart from conducting translational research and product development, we also act as a catalyst for advancements in the biopharma industry by facilitating technology transfers, and capability building through manpower development initiatives.

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Job Category: Research

Posting Date: 27 Mar 2025

Job Description:

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will support and participate in the SGH mission of providing quality patient care, education, and research.

Job Requirements:

1. Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
2. Fresh graduate or with at least one year of relevant experience
3. Proficient in using MS Office software
4. Effectively bilingual
5. Excellent oral and written communication skills

National Cancer Centre of Singapore Pte Ltd

Job Category: Research

Posting Date: 15 Jan 2025

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance with the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support and assist the Principal Investigator in the following trial-related activities:

• Patient screening and recruitment
• Monitoring subject’s compliance to their treatment and follow-up
• Data collection and management including resolving data discrepancies
• Coordinating the collection of biological specimens
• Monitoring of adverse events and safety reporting
• Maintaining and organizing investigator site files, preparation and submissions to the ethics committee and relevant local health authorities
• Tracking trial expenditures and timely invoicing

Requirements:

• Degree in Life Sciences/ Nursing/ Biomedical Science/ Biological Sciences
• 1-2 years of related working experience will be advantageous
• Good time-management and strong ability to multi-task
• Able to work independently and as a team
• Conscientious, meticulous, and self-motivated

National Neuroscience Institute of Singapore

Job Category: Research

Posting Date: 11 Jan 2025

We are looking for a candidate who will be providing research support service to the investigators in the conducting and implementation of clinical trial and/or clinical research studies at the National Neuroscience Institute (TTSH campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.

There will be opportunities to:

1. Contribute to clinical trials set-up, feasibility and coordination
2. Contribute to data processing and analysis of results for multiple studies conducted within the department
3. Acquire new skillsets, such as imaging handling, processing and analysis
4. Gain experience in scientific writing for presentations and publications

Requirements:

1. Bachelor’s degree in Life Sciences, Psychology or related fields
2. Good communications and interpersonal skills
3. Good IT literacy and statistics skills are also desirable
4. Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous