Total 3,139 job vacancies in George Town

The Medical Advisor primary responsibility is to oversee the design, implementation and conduct of some clinical studies for Moleac’s products. The responsibility may include local or international clinical trials for new registrations, new indications or line extensions for new or existing products.

It is expected that the Medical Advisor, in collaboration with academic experts and KOLs will contribute medical and scientific expertise needed to support state of the art development of Moleac’ products.

2. Responsibilities include to assist and provide input and collaborate with the marketing team in:

• a. Reviewing of different collaterals and communication support;
• b. Providing support for marketing events, presentations, scientific activities, and collaborations with speakers;
• c. Providing support in field intelligence and evaluation of data/publications to substantiate, update and improve the content of promotional messages and materials; and
• d. Reviewing accuracy of promotional messages and materials, including external communications materials such as scripts for marketing team, press releases, presentation during congresses, letters and positioning statements.

3. In liaison with Medical Affairs Team and Key Account Managers, the Medical Advisor is responsible to :

• a. Provide medically and scientifically suitable response to queries received on Moleac product from patients and/or families, physicians, partners, etc…
• b. Preparation of the response, follow-up to obtain additional clarifications, ensuring quick turnaround, and submitting the response for internal approval.
• c. Responsible for consistency and quality of the response: creating, maintaining, and updating of standard product response messages, medical information requests and responses.
• d. Pharmacovigilance
• e. Advising on the need to report the case as an AE.
• i. Gathering, evaluation, medical assessments and follow-up of adverse drug reaction events reported and of possible product complaints;
• ii. Review, monitor and track adverse drug reaction events reported for all products.

4. Additional responsibilities include, but are not limited to, driving publications, implementation and support of registry studies and other observational or real-world studies.

5. In addition, the Medical Advisor (Clinical Development), as part of the Medical Department Team, may be assigned to supporting Regulatory Affairs and Marketing teams as needed and in a timely manner, for specific projects.

The position is reporting to the Head of Clinical Development and Medical Affairs. It is mandatory that all activities be conducted with the highest ethical standards and scientific integrity, as well as compliance with applicable SOPs, guidelines, laws and regulations.


ESSENTIAL DUTIES & RESPONSIBILITIES
1. Clinical Trials under Moleac Drug Development Program (50%)

• Develops study concept, synopsis, full protocol, Investigator’s Brochure (IB), Informed Consent Form (ICF) and periodic safety report. Contributes medical expertise to CRF development, monitoring, data-management (DMP)and statistical analysis (SAP) plans
• Serves as Moleac liaison with KOLs, academic groups, advisory boards, investigators, etc. for study-related scientific and medical topics
• In liaison with Regulatory Affairs Department, ensure proper authorizations are obtained (Ethics Committee, IRB, Regulatory Authorities) to proceed with the assigned clinical studies
• Serves as scientific and medical advisor to provide guidance and support to Clinical Operations team, CRO/vendors and study sites personal on medical and scientific aspects of trials.
• Attends and/or presents at Kick-off meetings, Investigator’s Meeting, weekly team meetings, and vendor meetings, as needed or requested
• Performs medical review of collected data, and notably adverse events and concomitant medication coding, provide medical support for SAEs management. Performs review of Clinical Study Report (CSR) and patient narratives.
• Be available 24 hours per day, 7 days per week to respond to urgent protocol related issues at the investigative sites.

2. Additional responsibilities within Medical Affairs (35%)
As needed, and depending on workload, the incumbent will be assigned to contribute to some of the other activities pertaining to the Medical Affairs Department, and specifically:

• Provides in-depth perspective and support for existing and new registry platform. Ensures quality of data collection, produce reports from the registry in order to make presentations, publications, posters and promotional material
• Oversees and leads peer-reviewed publications activities at the level of an asset, ensuring robust planning and delivery as per marketing and commercial needs. Develops publication plans, develops publication materials, manuscripts and research articles for journal publication- Manages relationships with publishing houses.
• Responds to medical enquiries from Health Care Providers, partners, patients and other stakeholders

3. Support to Regulatory Affairs and Marketing teams (15%)
o Assist and provide input and collaborate with the marketing team in:

• Reviewing of different collaterals and communication support - conducting literature research to develop written materials
• Providing support for marketing events, presentations, scientific activities, and collaborations with speakers - Contributing to the development and implementation of briefings, trainings, and updates for the sales and marketing forces on products, diseases, and competition to enhance the overall understanding of the products, market environment as well as the regulations and guidelines that affect the products and services of the company.
• Providing support in field intelligence and evaluation of data/publications to substantiate, update and improve the content of promotional messages and materials; and
• Reviewing accuracy of promotional messages and materials, including external communications materials such as scripts for marketing team, press releases, presentation during congresses, letters and positioning statements.

o Assist Regulatory Affairs and Pharmacovigilance team in:

• Gathering, evaluation, medical assessments and follow-up of adverse drug reaction events reported and of possible product complaints;
• Creating, maintaining and updating of standard product response messages, medical information requests and responses.
• Review, monitor and track adverse drug reaction events reported for all products.

REQUIREMENTS
o Medical degree - Candidates with minimum 3 years’ experience with medical affairs roles and experience in neurology/neuroscience preferred.
o Strong scientific analytical and problem-solving skills, strategic capabilities, project management, planning and organizational skills with excellent communication, writing and presentation skills.
o Ability to interpret, evaluate and present clinical data to internal and external stakeholders. Ability to develop medical/scientific data into clear, teaching programs and plenary presentations.
o Ability to write and edit technical documents, such as protocols, informed consent, and other trial-related documents.
o Excellent verbal and written communications and presentation skills; fluent in written and verbal business English.
o Outstanding interpersonal and networking skills within and outside the organization.
o Ability to travel 40 – 50% of the time including overnight travel and willingness to visit remote or small cities across countries.

Interested applicants are invited to apply directly at the NUS Career Portal. Please note your application will only be processed if you apply via NUS Career Portal.

NUS Career Portal link: https://careers.nus.edu.sg/job/Assistant-Manager-%28Study-Monitor%29/33397-en_GB/

We regret that only shortlisted candidates will be notified.

Job Description

We are looking for an experienced clinical monitor to perform the study monitoring in the ADVANcing Clinical Evidence in Infectious Diseases Network (ADVANCE ID). ADVANCE ID is jointly funded by the Welcome Trust and Singapore institutions including the Saw Swee Hock School of Public Health and Yong Loo Lin School of Medicine, National University of Singapore. The vision of the Network is to improve public health by developing the clinical evidence base for the prevention and treatment of drug-resistant infections. Its mission is to build and sustain a strategic clinical research network focused on most efficiently delivering locally relevant interventions for drug-resistant infections.

The Network aims to improve and strengthen clinical research capabilities in the region by acting as a platform to develop good principles and practices. It will stabilise capacity and capabilities to mitigate inefficiencies in trial start-up phase and loss of skillset following study closure, as in typical trial setup. The Network will continuously develop its capabilities, quality and efficiency by learning from and collaborating with other clinical trial networks.

In the long term, the Network aims to support broader infectious disease studies by expanding geographically beyond its original starting point in South East Asia and collaborating with other networks around the world. It will function as an active network that involves patients in platform trials, allowing for rapid clinical research response in the event of an emerging infectious disease or pandemic threat.

The monitor should be able to supervise study sites and activities to ensure adherence to appropriate study protocols and applicable regulatory requirement terms of the study.

Duties & Responsibilities
•Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit reports.
•Monitor the progress of clinical study sites participating in a clinical study, and to assure the protocol is followed and data is reported accurately.
•Evaluate the quality and integrity of the reported data, site efficacy and investigational product (IP) management.
•Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
•Develop patient recruitment strategies in conjunction with the clinical site to meet enrolment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
•Assure that adverse events are correctly documented and reported.
•Ensure proper transmission of clinical case data to the data management centers, review case reports questions and problems and clarify or obtain alterations to data as appropriate.

Qualifications

•Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
•Ability to perform all clinical monitoring activities independently.
•Strong interpersonal, written, and verbal communication skills within a matrixed team.
•Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
•Good time management and ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
•Strong computer skills, including but not limited to the knowledge of an electronic data capture systems (EDC), Electronic Trial Master File (eTMF), Clinical Trial Management System (CTMS), and MS-Office products such as Excel and Word.
•BSc or MSc in relevant field. A lower educational credential may be considered if candidate has ample monitoring experience.

The Signature Research Programme in Emerging Infectious Diseases (EID) aims to pioneer our understanding of emerging infections through world-class research that integrates immunology, infection biology, pathogen genomics, and computational approaches. This integration drives comprehensive studies of host–pathogen interactions across molecular, individual, and population scales to address emerging health challenges. 
The Coronavirus Lab, led by Assistant Professor Mart Lamers within the Signature Research Programme in Emerging Infectious Diseases (EID), is seeking a full-time Research Fellow / Senior Research Fellow in Computational Biology. Our group leverages cutting-edge technologies—including organoids, CRISPR/Cas9, single-cell and spatial omics—to study coronavirus–host interactions that influence pandemic potential and disease pathogenesis.

We welcome applications from candidates with a strong background in computational and quantitative biology. The successful candidate will play a key role in analysing high-dimensional datasets and fostering an interdisciplinary research environment at the interface of virology, genomics, and data science.

We are looking for a creative, innovation-driven individual who is eager to uncover hidden patterns within complex datasets—insights that can both strengthen our experimental findings and spark bold, testable hypotheses that push the boundaries of discovery in our lab. This role also offers the freedom to develop quantitative AI/ML pipelines for pathogen risk assessment, informed by insights from our wet lab scientists.

Main Responsibilities

• Perform tasks and support all aspects of the research project.
• Carry out algorithm development and data analysis, including (but not limited to) single-cell and bulk transcriptomics, spatial omics, proteomics, and genome-wide association (GWAS) data independently.
• Lead AI/ML-driven efforts to develop pathogen risk assessment pipelines.
• Collaborate with experimental scientists to integrate computational findings with biological hypotheses.
• Contribute to scientific writing and dissemination of results through publications, presentations, and grant proposals.
• Mentor junior lab members and contribute to collaborative team science efforts.
• Perform other related duties incidental to the work described therein.

Job Requirements

• PhD Degree in a related scientific area (e.g., Bioinformatics, Computational Biology, Machine Learning/AI, Computer Science, Virology, Cell biology, or Immunology) with demonstrated hands-on experience in developing and/or applying algorithms for multi-omics data integration.
• Proven proficiency analysing bulk and single-cell transcriptomic datasets.
• Proficiency in R and/or Python coding.
• Familiarity with high-performance computing (HPC) environments and GPU programming.
• Have experience with spatial omics or GWAS analysis is strongly advantageous.
• Experience with AI/ML approaches for biological data analysis would be advantageous.
• Have excellent quantitative, analytical, and organizational skills.
• Collaborative, motivated, and adaptable, with a commitment to open and integrative team science.

We regret that only shortlisted candidates will be notified.

Job Description

We are looking for an experienced Network Engineer to manage, maintain, and support enterprise IT infrastructure across AIX, Linux, VMware, AWS, and database environments. The role will involve server administration, cloud infrastructure support, virtualization management, system monitoring, backup and recovery, performance tuning, and troubleshooting of infrastructure-related issues.

The successful candidate will be responsible for ensuring system availability, security, performance, and reliability across on-premise and cloud environments.

Key Responsibilities

Manage and administer AIX and Linux servers, including installation, configuration, upgrades, patching, migration, and maintenance.

Support enterprise server environments running on IBM AIX, RHEL, CentOS, Ubuntu, and related platforms.

Administer VMware ESXi and vCenter environments, including VM creation, cloning, templates, snapshots, vMotion, HA, and resource configuration.

Perform daily server health checks, monitoring of CPU, memory, disk, network, and system performance.

Troubleshoot server, operating system, network, hardware, and virtualization-related issues within agreed SLA timelines.

Manage user accounts, groups, permissions, file systems, security settings, and access controls.

Configure and manage LVM, NFS, Samba, LDAP, cron jobs, Apache, and other Linux/AIX services.

Perform backup, restore, disaster recovery, root password recovery, boot issue troubleshooting, and disk replacement activities.

Administer IBM Power Systems, including HMC, LPAR, DLPAR, VIO Server, SEA, MPIO, and NIM configuration.

Support AWS cloud infrastructure, including EC2, S3, IAM, VPC, RDS, CloudWatch, Route 53, EFS, security groups, Auto Scaling, and Load Balancers.

Create and manage AWS accounts, IAM access, EC2 instances, storage volumes, snapshots, backups, and cloud monitoring alerts.

Implement AWS security best practices using IAM, KMS, GuardDuty, AWS Shield, and related services.

Support cloud migration, cost optimization, automation, and high-availability cloud infrastructure.

Install, configure, and administer MySQL, MariaDB, Percona, PostgreSQL, Redis, and MongoDB in Linux environments.

Manage database users, schemas, backup jobs, replication, alerts, slow query settings, and database troubleshooting.

Support SAN storage administration, including LUN creation, expansion, mapping to ESXi, and health monitoring.

Use monitoring tools such as Nagios, Zabbix, Grafana, Cacti, and LPAR2RRD to track infrastructure health and performance.

Create scripts using Shell scripting, Bash, Korn shell, and Ansible playbooks to automate routine administration tasks.

Coordinate with internal teams, vendors, and support engineers for issue resolution, system maintenance, and infrastructure improvements.

Job Requirements

Diploma or Degree in Information Technology, Computer Science, Engineering, or related discipline.

Minimum 8 to 10 years of experience in system administration, infrastructure support, or related IT operations role.

Strong hands-on experience in AIX and Linux system administration.

Experience with Linux distributions such as RHEL, CentOS, and Ubuntu.

Good knowledge of VMware ESXi, vCenter, VM templates, cloning, snapshots, vMotion, and HA.

Hands-on experience with AWS cloud services, including EC2, S3, IAM, VPC, RDS, CloudWatch, Route 53, EFS, Load Balancers, and Auto Scaling.

Experience in server build, migration, upgrade, patching, monitoring, backup, and recovery.

Knowledge of IBM Power Systems, including HMC, LPAR, DLPAR, VIO, SEA, MPIO, and NIM will be advantageous.

Experience in MySQL, MariaDB, Percona, PostgreSQL, Redis, or MongoDB administration.

Knowledge of SAN storage, LUN mapping, ESXi storage connectivity, and storage health monitoring.

Familiar with monitoring tools such as Nagios, Zabbix, Grafana, Cacti, or LPAR2RRD.

Able to troubleshoot hardware, OS, network, storage, database, cloud, and virtualization issues.

Experience with automation tools such as Shell scripting and Ansible.

Good understanding of IT security, access control, backup strategy, disaster recovery, and system performance tuning.

Ability to work independently and as part of a team in a fast-paced environment.

Good communication, documentation, analytical, and problem-solving skills.

Professional certifications such as IBM Certified System p Administrator AIX, ITIL, AWS, Linux, or VMware certifications will be an advantage.

• Oversee daily restaurant and F&B operations, including front-of-house and back-of-house activities.
• Manage and supervise staff, including recruitment, scheduling, training, and performance evaluation.
• Monitor inventory levels, control costs, and prepare sales and operational reports.
• Ensure compliance with Singapore food safety regulations and company policies.
• Maintain high standards of customer service and resolve customer feedback or complaints promptly.
• Coordinate with suppliers and vendors to ensure smooth restaurant operations.
• Drive sales growth and implement strategies to improve operational efficiency and profitability.

Job Summary

About the Role

The Institute of High Performance Computing (IHPC), A*STAR, is seeking a highly motivated Research Scientist to conduct cutting-edge research in Healthcare AI Safety, Trustworthy AI, and Responsible AI Systems.

The successful candidate will lead the development of methodologies, frameworks, and technologies that ensure AI systems are safe, reliable, robust, transparent, and clinically trustworthy for deployment in healthcare settings. The role will focus on advancing AI safety research while enabling the responsible translation of AI innovations into clinical practice and healthcare operations.

Key Responsibilities

Research & Innovation

• Conduct original research in Healthcare AI Safety, Trustworthy AI, Machine Learning, and Artificial Intelligence.
• Develop novel methodologies and frameworks in areas such as:
• AI Safety and Alignment
• Trustworthy and Responsible AI
• Explainable and Interpretable AI
• AI Evaluation and Benchmarking
• Robustness and Reliability
• Human-AI Collaboration
• AI Governance and Risk Management
• Design techniques for detecting, mitigating, and monitoring AI failures, biases, hallucinations, and unsafe behaviors.
• Develop methods for uncertainty quantification, confidence estimation, and risk-aware decision-making.

• Develop safety frameworks for foundation models, large language models, multimodal AI systems, and agentic AI systems used in healthcare.
• Design methodologies to evaluate clinical safety, reliability, fairness, and generalizability of AI systems across diverse patient populations and healthcare settings.
• Develop monitoring systems for post-deployment surveillance, model drift detection, and continuous safety assessment.
• Build mechanisms for human oversight, escalation, and safe human-AI collaboration in clinical workflows.
• Develop evaluation frameworks for clinical decision support systems, healthcare copilots, and autonomous healthcare agents.
• Advance approaches for safeguarding patient privacy, data security, and responsible use of healthcare data.

Translational AI Safety

• Collaborate with clinicians, healthcare providers, regulators, policymakers, and industry partners to support safe deployment of AI systems.
• Contribute to healthcare AI governance frameworks, safety standards, regulatory science, and best practices.
• Translate AI safety research into practical tools, platforms, and operational frameworks for healthcare organizations.
• Support technology transfer, intellectual property generation, and commercialization opportunities.

Scientific Leadership

• Publish high-impact research in leading AI, machine learning, healthcare, and AI safety conferences and journals.
• Contribute to grant proposals, project planning, and strategic research initiatives.
• Mentor junior researchers, engineers, and students.
• Represent IHPC in collaborations with healthcare institutions, government agencies, regulators, and industry partners.

Requirements

Essential

• PhD in Computer Science, Artificial Intelligence, Machine Learning, Data Science, Biomedical Informatics, Healthcare Informatics, or a related discipline.
• Strong track record in AI/ML research demonstrated through publications, patents, or impactful projects.
• Strong programming skills in Python and modern machine learning frameworks such as PyTorch or TensorFlow.
• Experience developing and evaluating machine learning and deep learning models.
• Strong interest in AI safety, responsible AI, healthcare applications, and trustworthy AI systems.

Preferred

• Experience in one or more of the following areas:
• AI Safety and Alignment
• Trustworthy and Responsible AI
• Explainable AI (XAI)
• Foundation Models and Large Language Models
• Agentic AI Systems
• Healthcare AI and Clinical Decision Support
• AI Evaluation and Benchmarking
• Human Factors and Human-AI Interaction
• Regulatory Science and AI Governance
• Healthcare Data Privacy and Security

What We Offer

• Opportunity to shape the future of safe, trustworthy, and responsible AI in healthcare.
• Access to world-class computational infrastructure, healthcare datasets, and research facilities.
• Collaboration with leading AI researchers, clinicians, healthcare providers, regulators, and industry partners.
• A dynamic environment supporting both fundamental AI safety research and real-world deployment.
• Opportunities to influence national and international healthcare AI safety standards and frameworks

Career in the Hospital

Join our incredible team at the National University Hospital (NUH), where we believe that a hospital is more than just a workplace. Every day, we witness the remarkable impact that our healthcare professionals can have on individuals, families, and entire communities.

At NUH, we are driven by a shared purpose – to lend a helping hand to those in need, to be a source of support and healing, and to empower patients to live their best lives.

We are looking for passionate and committed individuals to join us as we transform lives and create a lasting impact in the lives of our patients. The impact you make at NUH will be profound, regardless of the role you take up in the hospital.

About NUH

The National University Hospital (NUH) is Singapore’s leading university hospital, with a proud heritage dating back to 1905 with the establishment of what’s now the NUS Yong Loo Lin School of Medicine. Our strong ties with the medical school have shaped us into a unique institution, allowing us to seamlessly integrate clinical care with teaching and research. As a university hospital, we go beyond the realm of providing tertiary medical care. We are a hub of knowledge and innovation, attracting healthcare professionals who are passionate about pushing boundaries and making significant contributions to the field.

About Department and Purpose of the Position

We are seeking a dynamic, resilient and highly dedicated Patient Service Associate to join our Specialist Outpatient Clinics.

As a Patient Service Associate, you will deliver friendly, efficient customer service and create a warm and welcoming atmosphere for our patients and visitors, with the key aim of providing excellence patient care and satisfaction.

Key Responsibilities

• Counter Registration
• Perform registration and screening of patients
• Perform accurate billing and timely collection of payments
• Comply to clinic facilities readiness
• Consultation Room
• Assist clinicians and/or therapists during clinic consultation.
• Provide proper care and coordination and coordinate first/follow-up appointments for patients.
• Manage wait time and keep patient updated in a timely manner.

Key Requirements

• Minimum “N” Level.
• Healthcare or service or related industry preferred but not required.
• Proficient in computer skills.
• Team player with good communication and interpersonal skills.
• Able to multitask and work in a fast paced environment.

Closing & Applications

When you join NUH, you become part of a dynamic and collaborative environment where expertise, knowledge, and compassion all come together.

Working in healthcare offers satisfaction that extend far beyond the ordinary. The smiles of gratitude from patients and the profound sense of fulfilment that comes from helping others cannot be measured. It is a career that allows for both personal and professional growth. The challenges you encounter in this rapidly evolving industry push you to constantly expand your knowledge and skills, as well as encourage lifelong learning.

Be a part of a team that gets to create a transformative healthcare experience for our patients and professionals alike.

The National University Health System (NUHS) is an integrated Academic Health System and Regional Health System in Singapore that delivers value-driven, innovative and sustainable healthcare. Institutions in the NUHS group include three hospitals – National University Hospital, Ng Teng Fong General Hospital and Jurong Community Hospital; three National Specialty Centres – National University Cancer Institute, Singapore, National University Heart Centre, Singapore and National University Centre for Oral Health, Singapore; a polyclinic group – the National University Polyclinics; one medical centre – Jurong Medical Centre; and three academic health sciences institutions – National University of Singapore (NUS) Yong Loo Lin School of Medicine (including the Alice Lee Centre for Nursing Studies), NUS Faculty of Dentistry and NUS Saw Swee Hock School of Public Health.

The Departments are seeking candidates who are highly motivated and willing to join us for a challenging and fulfilling appointment as Associate Consultant on a contractual basis.

As an Associate Consultant, you will be required to carry out the duties as directed by the Head of Department in accordance with the policies and guidelines set by the Hospital, National University Hospital (NUH) and the Ministry of Health (MOH).

You must be able to demonstrate good technical skills (i.e. operative and procedural skills where applicable).

•Possess a basic medical degree and a postgraduate qualifications relevant to the department’s specialty or nature of operations registrable with the Singapore Medical Council

•Be in active clinical practice

•Must be registered with the Singapore Medical Council and must be accredited as Specialists by the Specialist Accreditation Board, Ministry of Health

•Able to work independently with demonstrated competence in managing patients in the department

•Confident, takes initiatives and a good team player

The National University Health System (NUHS) is an integrated Academic Health System and Regional Health System in Singapore that delivers value-driven, innovative and sustainable healthcare. Institutions in the NUHS group include three hospitals – National University Hospital, Ng Teng Fong General Hospital and Jurong Community Hospital; three National Specialty Centres – National University Cancer Institute, Singapore, National University Heart Centre, Singapore and National University Centre for Oral Health, Singapore; a polyclinic group – the National University Polyclinics; one medical centre – Jurong Medical Centre; and three academic health sciences institutions – National University of Singapore (NUS) Yong Loo Lin School of Medicine (including the Alice Lee Centre for Nursing Studies), NUS Faculty of Dentistry and NUS Saw Swee Hock School of Public Health.

The Departments are seeking candidates who are highly motivated and willing to join us for a challenging and fulfilling appointment as Clinical Associate on a contractual basis.

As a clinical associate, you will be responsible for the total management of patients in the ward and administrative duties required of the department to provide direct patient care. In addition, you will be responsible for assisting the Registrar and Senior Staff in the running of the Specialist Outpatient Clinics.

•Be in active clinical practice •Possess a basic medical degree registrable with the Singapore Medical Council

•Possess a 3 year of post housemanship clinical experience

•Must be registered with the Singapore Medical Council

•Able to work independently with demonstrated competence in managing patients in the department

•Confident, takes initiatives and a good team player

Job Description:

As an academic health system, our combined resources allow you to leverage on our clinical excellence, research and education aspects of each institution in your pursuit of professional knowledge and expertise. You may from time to time be deployed to other institutions within of NUHS.

We are seeking candidates who are highly motivated and willing to join us for a challenging and fulfilling appointment as our specialist doctors.

As Consultant, you will be required to carry out the duties as directed by the Group/Chairman, Medical Board, Group Chief, Head of Department in accordance with the policies and guidelines set by the NUHS and the Ministry of Health (MOH).

Requirements:

· Possess a basic degree from a recognised medical school or Postgraduate which is registrable with the Singapore Medical Council;

· Completed the training and post-graduate qualifications which are recognised by the Specialists Accreditation Board (SAB);

· Active in clinical practice;

· Have at least 3 years of relevant experience as an accredited and licensed medical specialist;

· Able to work independently with demonstrated competence in managing patients, teaching and research in a multi-discipline environment;

· Confident, takes initiatives and a good team player.

Interested applicants are invited to apply directly at the NUS Career Portal. Please note your application will only be processed if you apply via NUS Career Portal.

NUS Career Portal link: https://careers.nus.edu.sg/job/Research-Fellow-%28Biological-Sciences%29/33316-en_GB/

We regret that only shortlisted candidates will be notified.

Job Description

The Molecular Breeding Laboratory at the Lee Hiok Kwee Functional Genomics Laboratories, Department of Biological Sciences led by Associate Professor Chew Fook Tim, is currently looking for TWO Research Fellows with relevant PhDs, and TWO Research Assistants with BSc(Hons) degree or MSc in relevant fields and background, to join the project on the Molecular Breeding of Leafy Greens and Fruiting Vegetables / Seed Innovation Hub.

The work would include:

• Large-scale Global Germplasm Evaluation and Assessment,
• Key Deep Phenotypic Definition and Evaluation, including molecular, cell culture-based and biochemical bioassays,
• Characterization of Genetic Control, Genome-wide Associations, and Functional Characterization of Candidates,
• Crossing, Cultivar and Lines Development,
• Integration of Genomic Data into Cultivation Processes,
• Multi-Location Trial Evaluations, 
• Project Management of External Collaborations, and
• Scientific Communications and Publications.

Qualifications

PhD Degree in Science and in related fields.

Skills:

• Strong motivation and leadership in pursuing challenging scientific questions.
• An ability to work well with interdisciplinary colleagues.
• Experience in mentoring and training junior researchers (including undergraduates and polytechnic interns).
• Excellent written and interpersonal communication skills.
• Good time and resource management skills.

Experience:

• Experience in Bioinformatics / Genetics / Statistics is mandatory and should be able to code in R.
• In addition, experience in Plant Molecular Biology techniques including CRISPR and Functional Characterization of Genetic Control, Large Scale -omics Technologies, and Data Analysis, would be an advantage.

Job Description:

• Design, develop, and validate new technology prototypes and proof-of-concept systems for 6G wireless networks.
• Implement and optimize wireless communication algorithms in lab and field environments.       
• Lead testbed system integration, including software and hardware co-development.        
• Oversee end-to-end system validation, verification, and performance benchmarking against relevant standards.
• Collaborate with ecosystem partners (infra. vendors, universities, labs) on prototyping and demonstration projects.

Requirements:

• MS or PhD in Electrical Engineering, Communication Engineering or related field.
• Strong DSP and wireless algorithm development skills; hands-on experience with system implementation.
• Deep understanding of mobile communication systems (3G, 4G, 5G, and beyond) and relevant specifications.
• Experience deploying prototypes and testbeds: programming proficiency in C/C++, Matlab, Python, Verilog, VHDL.
• Demonstrated ability to lead or work within multidisciplinary teams for wireless system development.
• Minimum 8 years of relevant Industry experience, ideally including practical demo or PoC achievements.
• Preferred expertise: AI-powered communications, satellite comms, or energy efficiency for wireless testbeds.

Interested candidates may apply through the application system. We regret that only shortlisted candidates will be notified.

PERSOL Singapore Pte Ltd • UEN No. 200007268E • EA License No. 01C4394 • EA Registration No. R22111378 (Ong Xin Yee)

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOL Singapore Pte Ltd and its affiliates to collect, use and disclose your personal data for the purposes set out in the Privacy Policy available at https://www.persolsingapore.com/policies. You acknowledge that you have read, understood, and agree with the Privacy Policy. 

Interested applicants are invited to apply directly at the NUS Career Portal. Please note your application will only be processed if you apply via NUS Career Portal.

NUS Career Portal link: https://careers.nus.edu.sg/job/Research-Fellow-%28Microbiology-&-Immunology%29/22121-en_GB/?st=8D4EEF9B0E1A95200D1286536EB80500394C0095

We regret that only shortlisted candidates will be notified.

Job Description

The National University of Singapore invites applications for Research Assistant for “Singapore Integrated Network for Genomic and Epidemiological Tick-borne Pathogen Investigation and Connectivity” in the Department of Microbiology & Immunology, Yong Loo Lin School of Medicine. The Department of Microbiology and Immunology (https://medicine.nus.edu.sg/mbio/) at NUS is dedicated to advancing research, teaching, and training in infectious diseases, immunity, and host-pathogen interactions. It is well known for strengths in immunology, virology, bacteriology, parasitology, and molecular biotechnology, supported by strong core research facilities and graduate training opportunities. Appointments will be made on a 1-year contract basis in the first instance, with the possibility of extension.

Purpose of the post

The Research Fellow (RF) will work closely with the Principal Investigator (PI) and study team to ensure timely, high-quality delivery of a tick and tick-borne disease biosurveillance project in Singapore. The RF will support end-to-end study operations, including coordination with study sites, participant/sample workflows, data management, analysis, and reporting, while maintaining strong professional standards and accurate documentation.

Main duties and responsibilities

The RF will liaise with relevant personnel across study sites (e.g., clinics/hospitals and partner units) to support smooth recruitment and data/sample collection processes and will be accountable to the PI. The RF will be able to:

1. Oversee the general management of the project, including planning, coordination and day-to-day troubleshooting to ensure milestones are met;
2. Provide administrative and secretarial support to the project, such as organizing regular meetings to maintain regular communication with other members of the research team and collaborate with the study sites;
3. Undertake the day to day running of the project at the study site, e.g. collaborate with team members at the study sites, support recruitment, coordinate field/site activities, and support data and/or sample collection at sites and relevant settings;
4. Conduct literature searches, support maintenance of the study database, perform data entry and cleaning, and analyse data using appropriate software tools; as well as assist in preparing both progress and final reports of the project;
5. Apply bioinformatics and AI-enabled approaches to support genomics and proteomics-related analyses as required by the study (e.g. use relevant bioinformatics tools and machine learning/deep learning workflows to support interpretation and reporting);
6. Maintain the highest standard of professional conduct and record keeping in accordance with policies and procedures, including accurate documentation and data integrity.

Qualifications

The applicant should:

1. Have a first degree with good results or holds a PhD degree in Biotechnology, Microbiology, Biochemistry, Molecular Biology;
2. Have a background in infectious pathogens and infection-related research, with training/exposure in microbiology, immunology and/or clinical microbiology, and experience working with pathogen-focused research questions;
3. Be able to work independently and in a team, have an investigative nature and attention to detail, and be able to deliver reports and presentations to stakeholders;
4. Have knowledge of computer applications and research software for data handling, analysis and reporting (e.g. MS Office/PowerPoint, EndNote/Mendeley, GraphPad Prism) and be familiar with computational/bioinformatics tools and workflows (e.g. machine learning approaches and sequence-based tools such as BLAST);
5. Have experiences in relevant areas of research spanning wet-lab and computational work, such as microbiology/molecular biology methods (e.g. biofilms, RNA extraction, RT-qPCR, ELISA, mammalian cell culture) and computational/AI methods (e.g. virtual screening/docking, molecular dynamics simulations, and machine learning model development).

Remuneration will be commensurate with the candidate’s qualifications and experience. Informal enquiries are welcome and should be made to Dr Benoit Malleret at benoit_malleret@nus.edu.sg.

Formal application: Please submit your application, indicating current/expected salary, supported by a detailed CV (including personal particulars, academic and employment history, complete list of publications/oral presentations and full contacts of three (3) referees to the NUS Career Portal.

We regret that only shortlisted candidates will be notified.

Interested applicants are invited to apply directly at the NUS Career Portal. Please note your application will only be processed if you apply via NUS Career Portal.

NUS Career Portal link: https://careers.nus.edu.sg/job/Research-Assistant-%28Microbiology-&-Immunology%29/20750-en_GB/?st=BBE292BB043DB988997818261DB218F6EFE0D99F

We regret that only shortlisted candidates will be notified.

Job Description

The National University of Singapore invites applications for Research Assistant for “Singapore Integrated Network for Genomic and Epidemiological Tick-borne Pathogen Investigation and Connectivity” in the Department of Microbiology & Immunology, Yong Loo Lin School of Medicine. The Department of Microbiology and Immunology (https://medicine.nus.edu.sg/mbio/) at NUS is dedicated to advancing research, teaching, and training in infectious diseases, immunity, and host-pathogen interactions. It is well known for strengths in immunology, virology, bacteriology, parasitology, and molecular biotechnology, supported by strong core research facilities and graduate training opportunities. Appointments will be made on a 1-year contract basis in the first instance, with the possibility of extension.

Purpose of the post

The Research Assistant (RA) will work closely with the Principal Investigator (PI) and study team members to support the successful completion of a tick and tick-borne diseases biosurveillance project in Singapore. The RA’s principal role will be to support field sampling and surveillance activities, manage and process study data for analysis and reporting, and contribute to accurate record-keeping and documentation to ensure project milestones are met on time.

Main duties and responsibilities

1. The Research Assistant will liaise with relevant personnel to facilitate the smooth running of fieldwork and related data workflows and will be accountable to the Principal Investigator (PI). The RA will be able to:
2. Provide administrative support to the project, such as organising regular meetings, maintaining communication with research team members and collaborators, and supporting scheduling and tracking of project tasks.
3. Support the day-to-day coordination of project activities, including planning and logistics for biosurveillance fieldwork across multiple sites in Singapore.
4. Provide administrative support to the project, such as organising regular meetings, maintaining communication with research team members and collaborators, and supporting scheduling and tracking of project tasks.
5. Assist with fieldwork operations at study sites, including supporting systematic collection activities and maintaining clear, consistent field records in line with project protocols.
6. Manage, clean, and process field and project data for analysis and reporting, maintaining well-organised datasets and contributing to the upkeep of project databases.
7. Support basic data analysis, visualisation, and reporting using relevant tools (e.g., MS Office, R Studio; ArcGIS where spatial outputs are needed), and assist with preparing progress updates and final reports.
8. Maintain high standards of professional conduct, data integrity, and record-keeping in accordance with project policies and procedures.
9. Assist with any other duties of a similar nature as delegated by the PI.

Qualifications

The applicant should:

1. Demonstrate competence in GIS-based mapping and spatial analysis (e.g., using ArcGIS), with the ability to support vector and tick-borne disease biosurveillance mapping and the integration of environmental and climate-related spatial data (e.g., satellite-derived indices, land cover, and other relevant layers) for analysis and reporting.
2. Have experience with field-based sampling and surveys, including working across varied habitats and maintaining accurate field notes, metadata, and sample documentation in accordance with project protocols.
3. Have a background in species identification and specimen handling, including experience with morphological documentation and/or contributing to species or ecological databases, with strong attention to detail in recording and data quality.
4. Have familiarity with molecular biology laboratory workflows relevant to biosurveillance (e.g., DNA extraction and PCR), and be able to follow laboratory protocols, maintain clear lab records, and support downstream identification workflows as required.
5. Be comfortable managing and organising datasets for analysis and reporting, and be proficient with standard productivity and data tools (e.g., MS Office), with added advantage of experience in analytical software (e.g., R).
6. Be able to work independently and collaboratively, with strong organisational and communication skills, and a professional approach to safety, confidentiality, and research integrity.

Remuneration will be commensurate with the candidate’s qualifications and experience. Informal enquiries are welcome and should be made to Dr Benoit Malleret at benoit_malleret@nus.edu.sg.

Formal application: Please submit your application, indicating current/expected salary, supported by a detailed CV (including personal particulars, academic and employment history, complete list of publications/oral presentations and full contacts of three (3) referees to the NUS Career Portal.

We regret that only shortlisted candidates will be notified.

Interested applicants are invited to apply directly at the NUS Career Portal. Please note your application will only be processed if you apply via NUS Career Portal.

NUS Career Portal link: https://careers.nus.edu.sg/job/Research-Fellow-%28Hybrid-organic-inorganic-perovskites%29/33365-en_GB/

We regret that only shortlisted candidates will be notified.

Job Description

The team of Prof Loh Kian Ping invites applications for a Research Fellow position working in the synthesis and characterization of hybrid organic inorganic perovskites single crystal and thin film. Our research focuses on engineering chirality and functionality on hybrid superlattices.  

Candidates with the following experiences will be advantaged:

(1)    the solution phase synthesis of large sized 2D hybrid organic inorganic perovskites crystals
(2)    Design of chiral or multiferroic 2D hybrid organic inorganic perovskites
(3)    Adept with the use of piezoresponse force microscopy to study ferroelectric phases
(4)    Adept with optical spectroscopic methods to study excitonic processes
(5)    Ability to solve single crystal XRD 

The candidate should have a PhD degree and strong track record in Materials Chemistry or Physics, with publishing in related areas.

An attractive renumeration package will be offered for suitable candidate with a strong record in 2-D condensed matter physics and who has good publication record.