789 Clinical jobs in Singapore

To closely work with patients and volunteers to recruit and coordinate participation in clinical studies. The ideal candidate should be able to liaise with team members, provide administrative support, and assist in database formation and data collection.

Key Responsibilities:

• Recruit and coordinate patient/volunteer participation in clinical studies.
• Liaise with research project team members for smooth project execution.
• Provide administrative and secretarial support for research projects, including organizing meetings and procurement of materials.

About the Opportunity:

We are a leading recruitment agency offering top-notch services to our clients and candidates alike.

Why This Role?

This role is perfect for individuals who want to make a meaningful impact in the pharmaceutical industry while working with a dynamic team.

What We Offer:

A supportive and collaborative work environment, opportunities for professional growth and development, and a competitive salary and benefits package.

How to Apply:

If you are a motivated and detail-oriented individual looking for a new challenge, please submit your application today.

This role involves close collaboration with patients and volunteers to recruit, coordinate and follow up on clinical studies.

• Patient/volunteer recruitment, coordination and follow-up for clinical studies
• Liaise and communicate with the research team to ensure smooth project execution
• Provide administrative support to research projects, including organizing meetings and procurement of materials
• Assist in clinical study database formation and data collection

The ideal candidate will possess excellent communication skills, experience in patient recruitment and coordination. Proficiency in Microsoft Office is also essential. Additionally, knowledge of healthcare principles is desirable.

The role of a Study Manager involves overseeing the planning and execution of clinical trials.

1. Create detailed timelines for study management activities.
2. Conduct risk assessments to ensure the success of clinical trials.
3. Develop and negotiate clinical study budgets with cross-functional personnel.

As the focal point of study-level communication, you will work closely with internal and external partners to develop and lead clinical studies.

You will also be responsible for determining and communicating Clinical Trial submission and approval requirements.

We are looking for a highly organized and detail-oriented individual who can manage multiple projects simultaneously and meet deadlines.

Key Responsibilities:

• Plan and execute study management activities
• Manage study development in partnership with internal and external partners
• Determine and communicate Clinical Trial submission and approval requirements

• Engage with Leaders and Regulators

• Opportunity to lead impactful projects

• Enhance Patient Care Quality

As a Manager, Clinical Quality Management, you will be responsible for the following duties:

• Lead and support the team in managing clinical data, quality assurance activities such as MOH licensing, audits, and safety walks.

• Oversee training and education initiatives focused on patient safety, clinical quality, and Infection Prevention and Control (IPC).

• Implement and monitor IPC programmes and drive clinical quality improvement projects.

• Develop, review, and uphold clinical standards to ensure consistent patient care quality.

• Assist the Director in liaising with senior management, department heads, and external agencies like MOH and AIC.

• Support departmental planning, reporting, and ongoing service development efforts.

• Mentor and supervise staff, while managing manpower planning and team growth.

• Help plan budgets and manage resources effectively.

• Take on additional projects or responsibilities as assigned by the Head of Department.

Requirements

• A degree in Medicine, Nursing, Allied Health, or Healthcare Management from a recognised institution.

• At least 5 years of relevant experience in healthcare operations or clinical quality management.

• Strong leadership and communication skills, with the ability to conduct training and manage teams effectively.

To apply, simply click on the ‘’apply’’ button in the job advertisement or alternatively, you can send in your resume via email

Email Address:

We regret to inform that only shortlisted candidates will be notified.

ALLIED SEARCH PTE. LTD.

EA LICENSE: 19C9777

Job Scope:

• Work closely with internal and external stakeholders across the care continuum to ensure care coordination, efficient care delivery, and removal of care barrier for patients
• Assist clinical and nursing team in the planning and logistic needs of the patients in the pretransplant setting
• Follow with patients after stem cell transplantation or cellular therapy treatment
• Conduct stem cell donor searches and facilitate donor identification process
• Coordinate appointments for donors and patients throughout various phases
• Ensure that all medical investigation results are generated timely
• Participation in Audit Preparation for the Haematopoietic Stem Cell Transplantation and Cellular Therapy Program
• Identify areas for improvement and develop quality improvement activities
• Assist in maintenance of clinical database

Job Requirements:

• Minimum Degree, preferably in Nursing / Allied Health / Science or equivalent
• Excellent interpersonal and communication skills
• Preferably with working experience in a similar setting
• Proficient in using MS office

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button

We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities

"Jobstudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties, please be aware of scams impersonating Jobstudio and our employees, you may call our office directly at 64221390 for verification. we will not be liable for loss arising from scams."

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Choong Yi Han

EA Personnel Reg No: R2196526

• Collection and completion of clinical data and clinical indicators in the master data
• Maintenance and timely completion of internal and external data reports
• Review of Care Standards and Document Control. Planning and facilitating clinical guidelines, SOPs and Forms within CQMU and for the clinical cluster.
• Plan and facilitate MOH licensing and re-licensing as appropriate.
• Conduct regular checks and audits, such as unplanned Admission Review, Mortality Review and Fall Prevention Audit etc.
• Arrange and coordinate and conduct at least monthly ward walks through the patient care and patient care related areas to identify risks, receive feedback from the ground staff and reiterate good and safe practices to the staff.
• Plan and facilitate training and education in the areas of clinical quality and safety and risks management.
• Arrange and coordinate mask fitting for the organisation, flu vaccination exercise and support the immunisation program.
• Provide secretariat support to Outbreak Management taskforce and ensure close follow-ups of all outstanding matters related to outbreak Management taskforce.
• Conduct regular Infection Prevention and Control (IPC) workshops @ RCLA.
• Identify areas for improvement through red flags in clinical indicators, audits and incident management.
• Oversee and manage the reporting and review of adverse events, medication errors, unplanned admissions, pressure injuries and serious reportable events and mortality including preparation and submission of reports.
• To develop clinical partnership with RHs & Research Institutes in research.

• Degree in Medicine / Nursing / Allied Health/Healthcare Management from a recognised institution is preferred.
• At least 5 years' experience in a related job scope in healthcare is preferred.
• Ability to conduct lectures, workshops and teaching sessions.
• Good communication skills, both oral and written.
• Good leadership qualities.
• Knowledge in Microsoft Word, Excel and PowerPoint.
• Good people management skills.

Clinical Trial Administrators play a crucial role in the planning and execution of study management activities. This includes developing timelines, managing risks, and monitoring budgets.

As the focal point of study-level communication between internal and external partners, you will serve as a key liaison to facilitate seamless collaboration.

Your responsibilities will include leading cross-functional personnel to develop and negotiate detailed clinical study budgets, as well as partnering with internal and external teams to lead study development.

To be successful in this role, you should possess a degree in a Science-related field and have preferred clinical trial admin experience.

The ideal candidate will have strong organizational skills, excellent communication abilities, and a keen eye for detail.

• Develop and execute study management plans
• Serve as the focal point of study-level communication
• Manage cross-functional personnel
• Partner with internal and external teams

The Manager assists the Director to oversee the Senior Executive /Executive in managing the department's operation.

A little about you and what we seek to accomplish together:

• Collection and completion of clinical data and clinical indicators in the master data
• Maintenance and timely completion of internal and external data reports
• Review of Care Standards and Document Control. Planning and facilitating clinical guidelines, SOPs and Forms within CQMU and for the clinical cluster.
• Plan and facilitate MOH licensing and re-licensing as appropriate.
• Conduct regular checks and audits, such as unplanned Admission Review, Mortality Review and Fall Prevention Audit etc.
• Arrange and coordinate and conduct at least monthly ward walks through the patient care and patient care related areas to identify risks, receive feedback from the ground staff and reiterate good and safe practices to the staff.
• Plan and facilitate training and education in the areas of clinical quality and safety and risks management.
• Arrange and coordinate mask fitting for the organisation, flu vaccination exercise and support the immunisation program.
• Provide secretariat support to Outbreak Management taskforce and ensure close follow-ups of all outstanding matters related to outbreak Management taskforce.
• Conduct regular Infection Prevention and Control (IPC) workshops @ RCLA.
• Identify areas for improvement through red flags in clinical indicators, audits and incident management.
• Oversee and manage the reporting and review of adverse events, medication errors, unplanned admissions, pressure injuries and serious reportable events and mortality including preparation and submission of reports.
• To develop clinical partnership with RHs & Research Institutes in research.

What you might need to have:

• Degree in Medicine / Nursing / Allied Health/Healthcare Management from a recognised institution is preferred.
• At least 5 years' experience in a related job scope in healthcare is preferred.
• Ability to conduct lectures, workshops and teaching sessions.
• Good communication skills, both oral and written.
• Good leadership qualities.
• Knowledge in Microsoft Word, Excel and PowerPoint.
• Good people management skills.

Department: Data Management and Statistics

Reports To: Associate Director, Biostatistics and Analytics

Location: Remote

Employment Type: Full-Time

The Clinical Data Analyst will play a key role in generating actionable insights through advanced data analysis and reporting. This position requires strong expertise in R programming, data visualisation, and automation to support informed decision-making across teams. The role contributes directly to enhancing the consistency, efficiency, and quality of data reporting within a clinical research or healthcare environment.

1. Develop and maintain automated reports and dashboards using R programming to support various stakeholders.
2. Standardize reporting tools and templates to ensure consistent presentation of clinical and operational data.
3. Create visualisations and conduct trend analyses to identify performance patterns and study-related insights.
4. Collaborate with cross-functional teams to gather requirements and deliver tailored analytical solutions.
5. Provide analytical support for forecasting, resource planning, and study metrics such as FTE and SDV.
6. Maintain thorough documentation of data processes, methods, and reporting protocols.
7. Monitor tool performance, identify bugs or inconsistencies, and coordinate resolution with relevant teams.
8. Support updates to SOPs, work instructions, and programming standards to align with current best practices.
9. Ensure adherence to applicable data protection regulations, quality standards, and internal policies.

• Timely and accurate delivery of reports and analytical tools
• Stakeholder satisfaction and engagement
• Percentage of automated reporting processes
• Quality and accuracy of data-driven projections
• Number of bugs/issues resolved
• Compliance with audit requirements and data standards
• Volume of self-initiated or support-driven projects
• Participation in training or knowledge-sharing initiatives

• Education: Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related quantitative field.
• Experience: 4-6 years of relevant experience in data analysis, ideally within a clinical research or healthcare setting.
• Technical Skills: Advanced R programming and data manipulation, automation and reporting tool development, data visualisation and interpretation, documentation and protocol writing, basic project management.
• Behavioural Competencies: Strong communication and collaboration abilities, detail-oriented with analytical thinking, effective problem-solving skills, time management, and ability to handle multiple priorities.

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