697 Clinical Research jobs in Singapore

Job Title: Clinical Research Associate

• Recruit and follow up with participants for clinical research studies.
• Manage research documentation, administrative duties, and data collection.
• Conduct study activities such as patient recruitment, data management, and electronic health record maintenance.
• Liaise with investigators, clinicians, and laboratory teams to set up clinical workflows.
• Prepare documentation for audits and coordinate IRB applications and annual reports.

Requirements:

• Bachelor's Degree in Science, Public Health, or Social Science.
• Ability to adapt to a fast-paced environment.
• Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA).

We welcome applicants with relevant experience. If you do not possess the required experience, your application will be considered on individual merits, and you may be contacted for other opportunities.

Research Assistant

The successful candidate will be responsible for patient recruitment, informed consent taking, and maintaining accurate records of study IDs. This role requires meeting daily and total patient recruitment targets, as well as traveling to all polyclinics for data collection. Additionally, the candidate will process patient reimbursement and assist with other duties delegated by the Principal Investigator.

To be considered for this role, applicants must hold a Diploma or Degree and possess strong interpersonal skills. Proficiency in MS Office applications is also essential.

• Patient Recruitment: Coordinate with patients to ensure timely and efficient recruitment into studies.
• Informed Consent Taking: Obtain informed consent from patients prior to participating in studies.
• Record Keeping: Maintain accurate and up-to-date records of study IDs and patient information.
• Travel: Travel to all polyclinics for data collection and patient recruitment.

• Patient Recruitment: You will be responsible for recruiting patients for our research studies. This involves approaching potential participants, explaining the study details, and obtaining informed consent.
• Data Collection: Once patients have given their consent, you will collect data from them through surveys and other means.
• Maintaining Patient Lists: You will maintain a master copy of the patient list to ensure accurate assignment of study IDs for surveys.
• Daily and Total Patient Targets: You will meet daily and total patient recruitment targets for the period of employment.
• Travel: You may be required to travel to all polyclinics for recruitment and data collection.
• Patient Reimbursement: You will process patient reimbursement, where necessary.

• Diploma Holder: A diploma in a relevant field is required.
• Strong Interpersonal Skills: You must possess strong interpersonal skills to effectively communicate with patients and colleagues.
• English Language Proficiency: You should be able to converse in English.
• MS Office Applications: You should be proficient in MS Office applications (Word, Excel & PowerPoint).
• Team Player: You should be a team player with excellent interpersonal and communication skills.
• Administrative and Project Management Skills: You should have strong administrative and project management skills, with the ability to manage multiple projects concurrently.

This role offers a range of benefits, including:

• Opportunity to work on diverse research projects
• Chance to develop your clinical research skills
• Collaborative and dynamic work environment

Please note that this job description is not exhaustive and you will be required to carry out other duties as delegated by the PI.

Key Responsibilities:

• Recruit and follow up with patients for clinical research studies.
• Conduct administrative tasks related to research studies, including data collection and management.

Required Skills and Qualifications:

• Diploma or equivalent in Science, Public Health, or Social Science with 3 years relevant experience.
• Bachelor's Degree in Science, Public Health, or Social Science with 3 years relevant experience.
• Excellent communication and interpersonal skills.
• Proficient in Microsoft Office applications.

This role presents an excellent opportunity for individuals interested in the healthcare industry to contribute to research studies. We welcome applicants who are eager to take on new challenges and work in a dynamic environment.

We are seeking a skilled Clinical Research Coordinator to join our team. As a key member of the research team, you will be responsible for managing and coordinating clinical research projects from start to finish.

Key Responsibilities:

• Collect and manage research data, including electronic health records.

• Set up and maintain investigator files and consent documentation.

• Maintain study databases such as REDCap and electronic medical records.

• Ensure strict adherence to study protocols, including HBRA compliance.

• Coordinate workflows across clinical departments for participant recruitment.

• Prepare documents for audits, IRB applications, amendments, and annual reports.

• Uphold professional conduct, data privacy, and compliance with institutional policies.

• Support the Principal Investigator (PI) and team with other research-related tasks as needed.

Requirements:

• Strong organizational and time management skills.

• Excellent communication and interpersonal skills.

• Ability to work independently and as part of a team.

• Experience with electronic health records and research databases.

• Knowledge of Good Clinical Practice (GCP) guidelines.

• Strong attention to detail and ability to meet deadlines.

Benefits:

• Opportunity to work in a dynamic and growing research environment.

• Chance to develop and grow your skills and expertise.

• Competitive salary and benefits package.

National Cancer Centre of Singapore Pte Ltd

Job Category: Research

Posting Date: 15 Jan 2025

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance with the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support and assist the Principal Investigator in the following trial-related activities:

• Patient screening and recruitment
• Monitoring subject’s compliance to their treatment and follow-up
• Data collection and management including resolving data discrepancies
• Coordinating the collection of biological specimens
• Monitoring of adverse events and safety reporting
• Maintaining and organizing investigator site files, preparation and submissions to the ethics committee and relevant local health authorities
• Tracking trial expenditures and timely invoicing

Requirements:

• Degree in Life Sciences/ Nursing/ Biomedical Science/ Biological Sciences
• 1-2 years of related working experience will be advantageous
• Good time-management and strong ability to multi-task
• Able to work independently and as a team
• Conscientious, meticulous, and self-motivated

National Neuroscience Institute of Singapore

Job Category: Research

Posting Date: 11 Jan 2025

We are looking for a candidate who will be providing research support service to the investigators in the conducting and implementation of clinical trial and/or clinical research studies at the National Neuroscience Institute (TTSH campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.

There will be opportunities to:

1. Contribute to clinical trials set-up, feasibility and coordination
2. Contribute to data processing and analysis of results for multiple studies conducted within the department
3. Acquire new skillsets, such as imaging handling, processing and analysis
4. Gain experience in scientific writing for presentations and publications

Requirements:

1. Bachelor’s degree in Life Sciences, Psychology or related fields
2. Good communications and interpersonal skills
3. Good IT literacy and statistics skills are also desirable
4. Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous

Job Responsibilities:

• Manage and execute clinical projects and related administrative tasks in a fast-paced environment.
• Ensure proper documentation and maintain an up-to-date database.
• Perform regular maintenance and calibration of clinical equipment.
• Handle data entry and collect accurate clinical data.
• Plan and schedule subject visits, including coordinating recruitment activities.

Job Requirements:

• Possess at least a Diploma or Degree in a relevant field.
• Able to work independently and meet tight project deadlines.
• Strong team player who can also work with minimal supervision.
• Capable of prioritizing tasks and managing multiple responsibilities efficiently.
• Excellent coordination, communication, and interpersonal skills.
• Able to thrive in a fast-paced environment and handle work-related stress effectively.

To apply for this position, please email your detailed resume, including your current and expected salary, to .

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

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• Assist the investigators in overall administration of clinical research activities prior to, during, and post-study, such as enrolling suitable subjects, taking vital signs, collecting and processing biological samples, collecting and entering data, and monitoring subjects’ condition.
• Work with the study team to ensure subjects’ safety.
• Carry out the required procedures according to the SOP, study protocol, and Instruction manual(s) in compliance with the Regulations and ICH Good Clinical Practice Guideline.
• Attend investigator’s meetings (local/overseas) and site initiation meetings as assigned, and liaise with relevant internal and external agencies during the course of work.

• Degree in Sciences/Nursing. Those with a Diploma will be considered as Associate.
• Registration with the Nursing Board, Singapore (applicable to State Registered Nurse only).
• At least 2 years’ experience in the coordination of clinical research activities.
• Good team player.
• Problem-solving skills.

Only shortlisted candidates will be notified.