560 Research Study jobs in Singapore
Research Study Associate
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Job Summary:
We are seeking a Research Study Associate to support investigator-initiated clinical studies.
Key Responsibilities:
- Screen, recruit and consent participants according to protocol; schedule and manage study visits and follow-ups;
- Prepare and maintain ethics submissions, regulatory documents and Investigator Site Files; support monitoring visits and audits;
- Administer assessments, collect data and ensure accurate and timely entry into study databases; assist with data cleaning and query resolution;
- Manage investigational products (e.g., essential oil blends, devices), track inventory and coordinate transport between study sites;
- Coordinate project timelines, budgets and reporting; assist in drafting progress reports and grant deliverables;
- Liaise with PIs, clinicians, collaborators and institutional partners; mentor junior CRC/RCS.
Requirements:
- Degree in Biomedical Science, Life Sciences, Nursing, Allied Health, Public Health or a related discipline;
- Minimum 3 to 5 years of experience in clinical research coordination, preferably in investigator-initiated trials;
- Strong knowledge of research ethics submissions (CIRB), regulatory requirements and visit/audit preparation;
- Proven track record in patient recruitment, participant engagement and study follow-up;
- Experience managing multiple concurrent studies and ensuring compliance with timelines and protocols;
- Proficient in Microsoft Office applications (Word, Excel, PowerPoint); familiarity with REDCap, SPSS or R is an advantage;
- Strong administrative and project management skills to support reporting, grant deliverables and stakeholder coordination;
- Excellent interpersonal and communication skills, with empathy for patients and caregivers;
- Highly organized, detail-oriented and able to work independently with minimal supervision;
- Proactive problem-solver with the ability to prioritize and manage competing demands;
- Team-oriented, with the ability to mentor junior CRCs/RCs;
- Flexible and adaptable, with willingness to work across sites (e.g., NCCS, SKH, community hospitals).
Research Study Manager
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Clinical research coordinators play a crucial role in ensuring the successful execution of clinical studies.
Key responsibilities include subject recruitment and follow-up , research documentation and administrative duties .
Research Study Support Specialist
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The Research Study Support Specialist plays a vital role in the success of research studies by coordinating patient recruitment, data collection, and management.
Main Responsibilities:
- Patient Selection: Identify eligible participants based on study criteria
- Consent and Data Collection: Obtain informed consent and administer relevant questionnaires
- Team Collaboration: Coordinate with research teams and clinicians to meet study objectives
- Project Management: Manage timelines and achieve research targets
- Data Management: Utilize databases like Redcap and hospital systems for efficient data collection and management
- Compliance: Ensure strict adherence to research protocols and regulations
Requirements:
- Minimum degree in Science, Public Health, or Social Science
- Strong communication and interpersonal skills
- No experience required; training will be provided
Scientific Research Professional
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The primary objective of this role is to contribute to the development and discovery of innovative methods for addressing emerging pathogens. This entails identifying new pathogens, developing diagnostic tools, treatments, and control strategies.
As a member of the BATPROTECT team, you will work closely with Prof Wang to elucidate the molecular mechanisms underlying bats' exceptional longevity and resistance to viral and age-related diseases. Key responsibilities include:
- Supporting all aspects of the research project
- Conducting accurate monitoring, documenting, and reporting of experimental results and/or research findings
- Assisting researchers in programming, data analysis, and literature review for various research projects
- Evaluating and interpreting collected data and preparing oral presentations or written reports/scientific manuscripts/literature for publication
- Contributing to project management, presentations, and publications of research work, including occasional laboratory demonstrations where applicable
For this position, we seek a candidate with a PhD in Life Sciences, Biology, Immunology, Biochemistry, or related fields, accompanied by prior experience in immunology or aging. The ideal candidate should demonstrate strong organizational and interpersonal communication skills, proficiency in written and verbal communication, and computer literacy.
Scientific Research Professional
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We are a cutting-edge research team dedicated to pioneering advancements in peptide screening, DNA/RNA analysis, and protein research.
Job Responsibilities:- Conduct peptide screening utilizing ELISA, bead-based separation, and other innovative techniques.
- Analyze DNA and RNA sequences through primer design, PCR, qPCR, purification methods including spin column, magnetic beads, ethanol precipitation, and phenol chloroform extraction. Additionally, perform electrophoresis using agarose gel and urea-PAGE, as well as NGS (Illumina).
- Examine proteins via SDS-PAGE, western blotting, and ELISA.
- Proficiency in peptide screening methodologies.
- Strong understanding of DNA/RNA analysis techniques.
- Able to operate various laboratory equipment.
We offer a dynamic work environment and opportunities for growth and development.
Associate Director, Scientific Research
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Associate Director, Scientific Research page is loaded# Associate Director, Scientific Researchlocations:
Singapore - Woodlands - NorthCoasttime type:
Full timeposted on:
Posted Todayjob requisition id:
41342-JOB# At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.# Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.# **Position Summary:**Illumina, a world-leading microarray and next generation sequencing (NGS) company, is seeking an Associate Director to lead the Singapore Assay R&D team. The successful candidate will lead in executing scientific R&D in the field of molecular biology and biochemistry to develop novel, best-in-class multiomics NGS products.The Associate Director will be part of a multi-disciplinary team working to execute the design and development of novel, robust products for Illumina sequencing platforms. They will be a strong technical and strategic contributor to the development of biochemistry and have a successful track record of working collaboratively on projects in a matrixed organization.Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.**Responsibilities:*** Develop and execute strategies focused on business excellence, aligning with the overall goals of the organization and company vision.* Directly manage, guide, coach and develop a team of scientists, managers and other staff to meet project milestones and business objectives.* Oversee day-to-day departmental operations, ensuring efficiency, quality, and compliance with company goals and standards.* Lead or support various projects, including technology transfers, new process implementation and scientific initiatives, often across multiple sites or globally, through ambitious goals and challenging tradeoff decisions while maintaining an energized and motivating work environment.* Liaise effectively and influence peers within departments and across the organization. Build and maintain close relationships with other functional groups in RnD, Process Engineering, Operations, Business Development, Product Management, and QA.* Recommend targets for new capabilities, technologies and initiatives, and drive evaluation and implementation of process improvements and technological integration.* Manage functional spending, budget creation, forecasting, and financial management activities for the department and its programs.* Prioritize, align and adjust resources to ensure success across multiple projects and priorities.All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities.**Qualifications and Skills:*** Demonstrated ability for strong leadership skills, including ability to lead teams, develop talent, and manage multiple priorities.* Proven ability to assess and organize complex information, solve ambiguous problems, and develop actionable strategies.* Excellent communication skills, including verbal, written and in presentation for effective engagement with diverse stakeholders.* Proven experience in the biotech or pharma industry, with a strong understanding of relevant product development, operational and regulatory landscapes.* Strong collaborative skills and ability to build relationships with global stakeholders.**Experience/Education:*** Requires PhD or equivalent, with a strong foundation in relevant scientific discipline such as Biochemistry, Molecular Biology, Genetics or related fields.* 10+ years of extensive experience in reagent and product development in biotech or pharmaceutical industry.# #
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact To learn more, visit: The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants.
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Scientific Officer/ Research Associate
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Job Description
Duke-NUS Medical School (Duke-NUS) was established through a landmark collaboration between two world-class institutions; Duke University and National University of Singapore, with the objective of providing innovative education and impactful research that enhance the practice of medicine in Singapore and beyond.
The Centre of Regulatory Excellence (CoRE) was established at Duke-NUS in 2014 with the mission of forming regional platforms and networks to grow competencies, build capacity and promote thought leadership in regulatory science and health policy in the Asia Pacific, with a focus on South-East Asia.
CoRE has established a strong and highly regarded education portfolio for industry professionals and regulators. The Centre also enables thought leadership and policy innovation in areas of health products regulation, and its expanded scope now includes issues related to global health, health policies and health system strengthening. Its key focus areas are digital health, vaccines & pandemic preparedness, advanced and innovative therapeutics, innovative clinical trials, and medical devices.
In 2023, Enterprise Singapore (EnterpriseSG) appointed CoRE to establish and lead the Standards Development Organisation (SDO) supporting the Biomedical and Health Standards Committee. CoRE is seeking a dedicated and experienced Scientific Officer to support the technical and operational functions of SDO. The successful candidate will play a key role in advancing national objectives related to the development and implementation of health product manufacturing standards, with the following key responsibilities:
- Identify industry needs and emerging trends for standard development in medical devices and quality management systems, aligned with Singapore Standards Council's objectives.
- Support the development and promotion of national and international standards in collaboration with industry partners.
- Review existing standards with stakeholders to ensure continued relevance and accuracy.
- Drive stakeholder engagement for standard adoption through events such as launches, conferences, and workshops.
- Support the administration and coordination of technical committees and working groups.
Qualifications
- Master's degree or MD/MBBS with at least 2 years' relevant work experience in healthcare regulation or medical devices quality management.
- Relevant work experience in health product regulation, medical devices, quality management systems, or standards development is preferred.
- Familiarity with digital health and the Singapore's healthcare innovation ecosystem.
- Strong project management and coordination skills.
- Excellent communicator – Written, Spoken and Presenting
- Highly organised, detail-oriented with strong interpersonal skills
- Adaptable and able to effectively multi-task and perform well under pressure, both independently and as part of a team, in a fast-paced and evolving environment.
- Demonstrates discretion, intellectual agility, and sensitivity to stakeholder dynamics
We regret that only shortlisted candidates will be notified.
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Scientific Officer/ Research Associate
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Overview
National University of Singapore – Central Singapore
Duke-NUS Medical School (Duke-NUS) was established through a landmark collaboration between Duke University and National University of Singapore, with the objective of providing innovative education and impactful research that enhance the practice of medicine in Singapore and beyond.
The Centre of Regulatory Excellence (CoRE) was established at Duke-NUS in 2014 with the mission of forming regional platforms and networks to grow competencies, build capacity and promote thought leadership in regulatory science and health policy in the Asia Pacific, with a focus on South-East Asia.
CoRE has established a strong and highly regarded education portfolio for industry professionals and regulators. The Centre also enables thought leadership and policy innovation in areas of health products regulation, and its expanded scope now includes issues related to global health, health policies and health system strengthening. Its key focus areas are digital health, vaccines & pandemic preparedness, advanced and innovative therapeutics, innovative clinical trials, and medical devices.
In 2023, Enterprise Singapore (EnterpriseSG) appointed CoRE to establish and lead the Standards Development Organisation (SDO) supporting the Biomedical and Health Standards Committee. CoRE is seeking a dedicated and experienced Scientific Officer to support the technical and operational functions of SDO. The successful candidate will play a key role in advancing national objectives related to the development and implementation of health product manufacturing standards, with the following key responsibilities:
Responsibilities
Identify industry needs and emerging trends for standard development in medical devices and quality management systems, aligned with Singapore Standards Council’s objectives.
Support the development and promotion of national and international standards in collaboration with industry partners.
Review existing standards with stakeholders to ensure continued relevance and accuracy.
Drive stakeholder engagement for standard adoption through events such as launches, conferences, and workshops.
Support the administration and coordination of technical committees and working groups.
Qualifications
Master’s degree or MD/MBBS with at least 2 years’ relevant work experience in healthcare regulation or medical devices quality management.
Relevant work experience in health product regulation, medical devices, quality management systems, or standards development is preferred.
Familiarity with digital health and the Singapore’s healthcare innovation ecosystem.
Strong project management and coordination skills.
Excellent communicator – Written, Spoken and Presenting
Highly organised, detail-oriented with strong interpersonal skills
Adaptable and able to effectively multi-task and perform well under pressure, both independently and as part of a team, in a fast-paced and evolving environment.
Demonstrates discretion, intellectual agility, and sensitivity to stakeholder dynamics
We regret that only shortlisted candidates will be notified.
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Data Collection Assistant
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Data Collection Assistant (Tuas), Contract
Responsibilities:
- Administration - Produce, update, and provide support on MS documents, databases, and other departmental systems; use expertise to help improve processes.
- Office and Organizational Skills - Ability to be resourceful and proactive, utilizing organizational skills and time management.
- Correspondence - Prepare emails, reports, agendas, and meetings notes as needed.
- Data Collection and Reporting - Collect and organize data using pre-set tools, methods, and formats to generate standard reports.
- Document Preparation - Prepare required documents and tracking using a variety of applications such as Microsoft Office and other standard office software.
- Data Compliance - Works to understand data collection, processing, and protection rules and regulations to achieve compliance that matches organization objectives and applicable laws.
- Business Meetings/Events Arrangement - Schedule appointments, arrange meetings and conferences, and organize travel plans, as needed.
- Operational Compliance - Develop knowledge and understanding of the organization's policies and procedures and of relevant regulatory codes and codes of conduct to ensure adherence to those standards.
- Procurement - Support others by carrying out a range of procurement activities.
- Other duties as assigned
Requirements:
- Verbal Communication - Uses clear and effective verbal communication skills to express ideas and request actions.
- Planning and Organizing - Works with guidance to plan, organize, and prioritize activities to efficiently meet business objectives.
Kang Abelene Marianne Mrs Rozario Abelene Marianne
EA License No.: 02C3423 | Personnel Reg No.: R
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Statistical Specialist, Data Collection, MRSD
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Ministry of Manpower
Permanent/Contract
What the role is
The position is located in the Manpower Research and Statistics Department (MRSD), Singapore. The department produces a wide range of national labour market statistics to facilitate informed decision-making within the government and the community-at-large.
What you will be working on
The candidate will be part of the Data Collection team. Responsibilities include:
• Plan and coordinate official surveys, ensuring they are completed with high response rates
• Provide guidance and advice to survey interviewers to ensure that surveys are conducted in a timely and reliable manner
• Coordinate with various stakeholders to provide solutions for escalated cases
• Analyse macro trends to detect outliers and anomalies
• Use data analytical tools to conduct validation checks on data to ensure that it is accurate
• Provide regular updates of survey statistics and data quality to senior management
What we are looking for
• Excellent communication and interpersonal skills
• Strong analytical and quantitative skills
• Comfortable with working with diverse groups of people
• Self-starter who is able to thrive in a fast-paced environment
• Knowledge of Python, R or Tableau is an advantage
PWDs are welcome to .
About Ministry of Manpower
Championing Human Potential for a Thriving Singapore
Singaporeans are at the heart of what we do. The Ministry of Manpower (MOM) empowers our people and fosters a thriving, inclusive workforce that drives Singapore's growth and prosperity. By working closely with our tripartite partners, industry and community stakeholders, we strive to create workforce and workplace policies that foster resilience, adaptability, and a bright future for a thriving Singapore.
As an MOM officer, you will be part of this meaningful mission, contributing across diverse and impactful areas - from shaping forward-looking and effective manpower policies and strengthening industrial relations, to enhancing workplace safety standards and ensuring balanced local and foreign workforce regulations. Here at MOM, we are committed to creating an inclusive experience not just for our national workforce, but also for our officers who work tirelessly to champion human potential for a thriving Singapore.
About your application process
If you do not hear from us within 4 weeks of the job ad closing date, we seek your understanding that it is likely that we are not moving forward with your application for this role. We thank you for your interest and would like to assure you that this does not affect your other job applications with the Public Service. We encourage you to explore and for other roles within Ministry of Manpower or the wider Public Service.