38 Research Participant jobs in Singapore

Location: Buona Vista
Salary: $30/hr
Working hours: Mon-fri, Office hours

Responsibilities:

• Provides assistance to the research team

• Screens and recruits suitable patients to participate in the research project

• Briefs patients on research background and rationale and to obtain their consent of participation

• Collects data from patients' medical records and research statistics

• Helps document adverse events / reactions that arise

• Performs phlebotomy and venepuncture when required

Requirements:

• Minimum Degree/ Diploma in Nursing

• Min 3 years' experience in Hospital

If interested, please send me your most updated resume to WA: or email me at:

All candidates' information will be treated with the strictest confidence

Katherine Carlen

CEI.No: R

Recruit Express Pte Ltd

EA Licence No: 99C4599

Location: Buona Vista
Salary: $30/hr
Working hours: Mon-fri, Office hours

Responsibilities:

• Provides assistance to the research team

• Screens and recruits suitable patients to participate in the research project

• Briefs patients on research background and rationale and to obtain their consent of participation

• Collects data from patients' medical records and research statistics

• Helps document adverse events / reactions that arise

• Performs phlebotomy and venepuncture when required

Requirements:

• Minimum Degree/ Diploma in Nursing

• Min 3 years' experience in Hospital

If interested, please send me your most updated resume to WA: or email me at:

All candidates' information will be treated with the strictest confidence

Katherine Carlen

CEI.No: R

Recruit Express Pte Ltd

EA Licence No: 99C4599

We are seeking a skilled Clinical Research Coordinator to manage research projects at a reputable hospital in Singapore.

Key Responsibilities:

• Recruit and follow up with participants for various research studies
• Conduct data collection and management tasks, including extracting information from electronic health records
• Maintain accurate study records in databases and electronic health record systems
• Liaise with investigators, clinicians, and laboratory teams to develop clinical workflows

Requirements:

• A degree in Science, Public Health, or Social Science is preferred
• The ability to adapt to a dynamic work environment is essential
• Familiarity with Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA) is required

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.
#J-18808-Ljbffr

Responsibilities
Provides assistance to the research team
Screens and recruits suitable patients to participate in the research project
Briefs patients on research background and rationale and to obtain their consent of participation
Collects data from patients' medical records and research statistics
Helps document adverse events / reactions that arise
Performs phlebotomy and venepuncture when required
Requirements
Minimum Degree/ Diploma in Nursing
Min 3 years’ experience in Hospital
Only Nurses with SNB license NEED APPLY
Interested candidates please send a copy of your resume in MS Word to

Cameron Tan
Outsourcing Team
Company Reg. No. W
EA Licence No. 99C4599
#J-18808-Ljbffr

Responsibilities:

• Provides assistance to the research team

• Screens and recruits suitable patients to participate in the research project

• Briefs patients on research background and rationale and to obtain their consent of participation

• Collects data from patients' medical records and research statistics

• Helps document adverse events / reactions that arise

• Performs phlebotomy and venepuncture when required

Requirements:

• Minimum Degree/ Diploma in Nursing

• Min 3 years’ experience in Hospital

Only Nurses with SNB license NEED APPLY

Interested candidates please send a copy of your resume in MS Word to

Cameron Tan

Outsourcing Team

Company Reg. No. W

EA Licence No. 99C4599

Location: Buona Vista
Salary: $30/hr
Working hours: Mon-fri, Office hours

Responsibilities:
• Provides assistance to the research team
• Screens and recruits suitable patients to participate in the research project
• Briefs patients on research background and rationale and to obtain their consent of participation
• Collects data from patients' medical records and research statistics
• Helps document adverse events / reactions that arise
• Performs phlebotomy and venepuncture when required

Requirements:
• Minimum Degree/ Diploma in Nursing
• Min 3 years’ experience in Hospital

If interested, please send me your most updated resume to WA: or email me at:

All candidates’ information will be treated with the strictest confidence

Katherine Carlen

CEI.No: R

Recruit Express Pte Ltd

EA Licence No: 99C4599

Job Summary:

We are seeking a Research Study Associate to support investigator-initiated clinical studies.

• 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.

• 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).

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 .