459 Clinical Research jobs in Singapore

Job Title: Clinical Research Associate

We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Research Associate.

Responsibilities:

• To assist the principal investigator in developing and implementing clinical research protocols
• To prepare and submit regulatory documents for approval
• To facilitate the signing of project agreements with external collaborators
• To implement and monitor programme activities and workflow
• To conduct surveys or questionnaires
• To manage study-related equipment and handle queries from research subjects

Requirements:

• Degree in Nursing, Biological Science, Pharmacy or other healthcare related discipline
• Able to work independently and adapt in a fast-paced environment

Benefits:

This role offers the opportunity to work on exciting clinical research projects and develop valuable skills in clinical trials management. If you have a passion for research and are looking for a challenging role, we encourage you to apply.

Contact Information:

Please send your resume to for consideration.

Seeking a highly skilled and dedicated Research Fellow to join our team.

As a Research Fellow, you will play a key role in supporting the design, execution, and analysis of clinical and translational research projects.

Main Responsibilities

• Design and refine clinical or population-based research protocols to ensure high-quality results.
• Collaborate with clinicians, data analysts, lab personnel, and institutional research offices to implement efficient study protocols.
• Develop study objectives, inclusion criteria, methodology, and outcome measures through collaborative efforts.
• Propose new studies by planning, preparing study protocols, and implementing these studies efficiently.
• Conduct statistical analyses, clean, and interpret datasets using advanced statistical tools.
• Prepare and present data and insights at various relevant forums to drive decision-making.
• Collaborate on manuscript preparation for submission to peer-reviewed journals through literature review, data analysis, and drafting.
• Provide guidance to junior research staff, interns, or medical students supporting the project.

Additional Responsibilities

• Work closely with cross-functional teams to bridge clinical and scientific information into actionable insights.
• Attend regular team meetings, journal clubs, and collaborative planning sessions to drive project success.
• Stay up-to-date with industry trends and best practices to continuously improve research methods and outcomes.

• Collaborate with the Principal Investigator to secure and manage grant funding.
• Oversee the coordination of studies across multiple sites.
• Assist in monitoring project progress and coordinating regular reviews with the study team.
• Develop and prepare study-related presentations and materials.

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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

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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.

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

• 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.

• 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.

Job Summary:

This role involves coordination and administration of research studies, focusing on recruitment, data collection, and management.

Key Responsibilities:

• Participate in subject recruitment, scheduling, and data entry processes, adhering to study protocols.
• Screen patients based on eligibility criteria and communicate the study's objectives in a clear and concise manner.
• Obtain informed consent, administer study questionnaires, and ensure timely follow-up with study participants.
• Collaborate closely with the research team, clinicians, clinic staff, and relevant departments to guarantee research study needs are met.
• Manage multiple tasks simultaneously, set realistic targets, and achieve research deliverables within tight timelines.
• Conduct research activities including patient recruitment, data collection, and data management.
• Assist in extracting data from electronic health records and maintain accurate records in databases such as Redcap and electronic health record systems.
• Maintain adherence to strict research protocols, including those related to patient confidentiality and data security.
• Liaise with investigators, clinicians, and laboratory teams to establish efficient clinical workflows at various departments for research recruitment purposes.
• Prepare necessary documentation for audit purposes and coordinate submissions of new IRB applications, study amendments, and annual reports.
• Ensure highest standards of professional conduct, record-keeping, and adherence to hospital policies, ethics requirements, and local regulations.