729 Clinical Research jobs in Singapore

We are seeking a highly skilled and organized Clinical Trial Coordinator to join our team. The successful candidate will have a strong foundation in life sciences, with excellent organizational and documentation skills.

The role requires the ability to prepare and submit clinical trial documents, maintain accurate records, and ensure compliance with regulations.

Key responsibilities include:

1. Preparing, drafting, submitting, and tracking clinical trial documents for submissions, amendments, and approvals.
2. Maintaining accurate records of IEC correspondence, approvals, study documentation, and trial records.
3. Coordinating with sponsors, investigators, and internal teams to provide timely project updates.
4. Supporting study start-up activities, including preparation of consent forms, subject information sheets, and protocol compliance.
5. Assisting in audits, inspections, and quality management processes.
6. Recruiting and screening participants for assigned clinical trial projects.
7. Managing participant inclusion, scheduling, and ensuring smooth study execution.
8. Performing skin-related measurements and operating clinical research equipment.
9. Overseeing equipment maintenance, calibration, and proper usage.
10. Managing product storage, accountability, destruction, and other ad-hoc clinical trial inventory requirements.

This is an exciting opportunity to grow your career in clinical trials. If you have experience in clinical trials, IEC/IRB submissions, or regulatory compliance, we encourage you to apply.

• Strong foundation in life sciences
• Excellent organizational and documentation skills
• Ability to prepare and submit clinical trial documents
• Accurate record-keeping and compliance with regulations
• Strong communication and teamwork skills

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

Job Title: Clinical Research Associate

About the Role:

The successful candidate will play a key role in the coordination and conduct of clinical research studies. This includes recruiting and screening patients, explaining study goals clearly, obtaining consent, administering questionnaires, and following up with participants.

The ideal candidate will have excellent communication and interpersonal skills, as they will be working closely with research teams, clinicians, and clinic staff to meet study needs.

Responsibilities:

• Recruit and screen patients based on study eligibility.
• Coordinate with research teams, clinicians, and clinic staff to meet study needs.
• Manage data collection and ensure strict compliance with research protocols and regulations.
• Work with investigators and labs to set up clinical workflows for recruitment.
• Prepare documents for audits and assist with IRB submissions and reports.

Requirements:

• Min. Degree in Science/ Public Health/ Social Science or any relevant field.
• Adaptable, strong communication and interpersonal skills.
• No experience as training will be provided.
• Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA).

We are seeking a highly skilled and motivated individual to fill the role of Research Assistant. The successful candidate will be responsible for assisting Principal Investigators and site-PIs with various research projects.

1. Liaising with Principal Investigators and site-PIs to coordinate research activities.
2. Coordinating with various departments for clinical research procedures.
3. Ensuring adherence to protocol procedures.
4. Screening and recruiting suitable candidates as research participants.
5. Explaining protocols to research participants and ensuring informed consent is obtained in accordance with ICH GCP and HBRA requirements.
6. Contacting and scheduling appointments for research subjects within specified timeframes.
7. Centrifuging blood specimens and sending them to laboratories.
8. Tracing and returning case notes, blood results, and other required documentation.
9. Collecting data and performing research procedures.
10. Maintaining patient reimbursement logs, hardcopy and electronic case report forms.
11. Documenting source data for each patient according to protocol requirements.
12. Identifying, documenting, and submitting protocol deviations to IRBs according to hospital and sponsor procedures.
13. Informing PIs and collaborators on adjustments based on protocol changes.
14. Completing, reporting, and following up on unanticipated problems involving risk to subjects and adverse events/serious adverse events.
15. Collaborating with the Research Database IT Specialist on extracting patient medical records and data mining.

Additionally, general responsibilities include:

• Participating in projects and activities assigned by the Director, Clinical Research Unit.
• Working collaboratively with the research team to achieve project goals.

Required skills include:

• Machine Learning.
• Cell Culture.
• Psychology.
• Data Analysis.
• Clinical Research.
• Medicine.
• Recruiting.
• Data Mining.
• Python.
• Molecular Biology.
• Screening.
• Medical Records.
• Laboratory.

Minimum Diploma in Biomedical Science or equivalent.

Experience as a Research Assistant preferred.

The ideal candidate should possess excellent communication and interpersonal skills.

Strong organizational and time management skills are essential.

Able to work effectively in a team environment.

Highly adaptable and able to prioritize tasks efficiently.

Excellent analytical and problem-solving skills.

Proficient in Microsoft Office applications, including Word, Excel, and PowerPoint.

Knowledge of laboratory software and equipment an asset.

Job Summary:

We are seeking a skilled Research Coordinator to join our research team. The successful candidate will be involved in qualitative and/or quantitative research, working closely with study participants and the research team.

Key Responsibilities:

• Conduct patient education sessions
• Obtain informed consent from participants
• Perform interviews and collect data
• Evaluate and investigate research findings
• Record and maintain accurate records
• Ensure equipment is properly maintained and resources are optimized
• Schedule appointments and prepare set-ups
• Coordinate and liaise with study participants and the research team
• Review, compile, and send data or reports
• Monitor progress and update records
• Ensure compliance with study protocols and established procedures

Required Qualifications:

• A degree or diploma in physiotherapy or a relevant academic certification
• At least 2 years of experience for Diploma-holders
• Proficiency in MS Office software
• Prior experience in qualitative transcription and conducting qualitative interviews is preferred

Desirable Skills:

• Quantitative Research Methods
• Clinical Research Experience
• Excellent Interpersonal Skills
• Treatment Planning
• Healthcare Administration
• Patient Education Techniques
• Data Entry Skills
• MS Office Proficiency
• Clinical Trials Management
• Protocol Development
• Compliance and Auditing
• Office Software Expertise
• Nursing Principles
• Life Sciences Knowledge
• Screening and Scheduling
• Transcription Services
• IRB Compliance

Job Description:

We are seeking a detail-oriented and organized Clinical Research Coordinator to support the success of our studies.

The ideal candidate will have excellent communication skills, be able to work independently and as part of a team, and have a strong attention to detail.

Responsibilities:

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• Recruit and schedule study participants; screen for study eligibility.
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• Explain study objectives to potential participants in layman terms and obtain informed consent.
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• Administer study questionnaires and conduct follow-up with study participants.
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• Collaborate with clinicians, research teams, and clinic staff to ensure study needs are met.
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• Carry out study procedures including patient recruitment, data collection, and data entry.
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• Extract data from electronic health records (EHR) and maintain study databases (e.g., REDCap).
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• Set up and manage investigator files and consent records.
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• Coordinate IRB submissions, amendments, and annual reports.
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• Ensure full compliance with study protocols and regulations (e.g., HBHRA).
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• Support audits and maintain proper research documentation.
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• Work closely with investigators, clinicians, and labs to set up workflows for recruitment across departments.
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Requirements:

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• Bachelor's degree in a related field.
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• 1-2 years of experience in clinical research or a related field.
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• Excellent communication and organizational skills.
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• Ability to work independently and as part of a team.
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• Detail-oriented and able to maintain accurate records.
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Benefits:

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• Opportunity to work on exciting research projects.
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• Professional development opportunities.
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• Collaborative and dynamic work environment.
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What We Offer:

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• A competitive salary and benefits package.
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• The opportunity to work on a variety of research projects.
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• A dynamic and collaborative work environment.
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Key Responsibilities:

• Conduct clinical research activities, including patient recruitment and data collection.
• Maintain accurate and detailed records of research study progress.
• Communicate effectively with research team members, clinicians, and other stakeholders to ensure successful study outcomes.

• Bachelor's degree in a life science or related field.
• Excellent communication, organizational, and problem-solving skills.
• Able to work independently and as part of a team.

• Promoting knowledge and expertise through training and development opportunities.
• Collaborative work environment that fosters teamwork and innovation.
• Opportunities for career advancement and professional growth.

At our organization, we value dedication, hard work, and teamwork. If you are passionate about contributing to the success of our research endeavors, we encourage you to apply for this exciting opportunity.

Overview

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

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

• Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
• Fresh graduate or with at least one year of relevant experience
• Proficient in using MS Office software
• Effectively bilingual.
• Excellent oral and written communication skill
• Excellent interpersonal skill

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Job Category: Research

Posting Date: 27 Mar 2025

Job Description:

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

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

Job Requirements:

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