574 Clinical Research Professionals jobs in Singapore

Clinical Research Coordinator

Job Description:

• We are seeking a highly motivated and organized Clinical Research Coordinator to support our research projects. The ideal candidate will have excellent communication and interpersonal skills, with the ability to work effectively in a team environment.
• The Clinical Research Coordinator will be responsible for coordinating all aspects of clinical trials, including participant recruitment, data collection, and reporting.
• This is an exciting opportunity for someone who is passionate about healthcare and research to join our team and contribute to the development of new treatments and therapies.

About This Role

• Screen and recruit participants according to protocol eligibility and assist investigators in explaining study objectives and procedures.
• Verify participant eligibility and obtain informed consent prior to study enrolment.
• Schedule and conduct study visits in line with protocol; ensure participant compliance and follow-up.
• Manage accurate and timely data collection, entry, and maintenance of tracking logs and study documentation.
• Monitor and report adverse events, protocol deviations, and abnormal findings to PI and relevant authorities.
• Coordinate and support monitoring visits, audits, and follow-up actions.
• Liaise with research teams for smooth project coordination; provide regular updates and attend team meetings.
• Support regulatory and ethics submissions; draft correspondence with authorities as needed.
• Oversee study site setup, logistics, and investigator file preparation for study initiation.
• Track study budgets and payments; manage multi-site coordination where applicable.
• Assist in preparation of presentations, study materials, and evaluation of research findings.

Key Skills and Qualifications

• Excellent communication and interpersonal skills.
• Ability to work effectively in a team environment.
• Strong organizational and time management skills.
• Attention to detail and accuracy.
• Knowledge of clinical research principles and practices.
• Ability to maintain confidentiality and handle sensitive information.

Benefits

• Opportunity to work on exciting and challenging research projects.
• Chance to develop new skills and gain experience in clinical research.
• Collaborative and dynamic work environment.
• Competitive salary and benefits package.

How to Apply

Our client is expanding their clinical operations team and is looking for a Clinical Research Associate / Clinical Operations Associate to support the planning and execution of ongoing and upcoming clinical studies. The head office is based in the United States, with a Singapore clinical research branch established in the western region of Singapore.

Key Responsibilities:

• Support day-to-day management and execution of clinical trials in Singapore
• Conduct and document site monitoring visits(pre-study, initiation, routine, and close-out)
• Assist in the development of trial protocols, CRFs, and related study documentation
• Coordinate ethics submissions and regulatory applications (IRB / HSA)
• Track investigational product and trial materials to ensure compliance with GCP and SOPs
• Provide project management support — tracking timelines, vendors, and procurement activities
• Collaborate closely with internal scientists, regulatory staff, and external clinical partners
• Oversaw coordination of project extensions with the CRO, facilitating communication between the Singapore and US headquarters, research centres, hospitals and pharmaceutical stakeholders

Requirements:

• Bachelor's degree in Life Sciences, Medical Sciences, or related field
• 2–5 years of experience in clinical research, clinical operations, or trial coordination
• Practical experience in site monitoringand strong understanding of ICH-GCP
• Organized, meticulous, and proactive with excellent documentation habits
• Clear communicator with the ability to work independently in a small, agile team
• Exposure to project or program management is a plus

Why Join Us

• Be part of a mission-driven biotech tackling rare diseases from Singapore
• Work in a hands-on, cross-functional environment where your contributions matter
• Competitive salary and benefits package
• Growth opportunities into clinical operations, project management, or regulatory pathways

Our client is expanding their clinical operations team and is looking for a Clinical Research Associate / Clinical Operations Associate to support the planning and execution of ongoing and upcoming clinical studies. The head office is based in the United States, with a Singapore clinical research branch established in the western region of Singapore.

Key Responsibilities:

• Support day-to-day management and execution of clinical trials in Singapore
• Conduct and document site monitoring visits(pre-study, initiation, routine, and close-out)
• Assist in the development of trial protocols, CRFs, and related study documentation
• Coordinate ethics submissions and regulatory applications (IRB / HSA)
• Track investigational product and trial materials to ensure compliance with GCP and SOPs
• Provide project management support — tracking timelines, vendors, and procurement activities
• Collaborate closely with internal scientists, regulatory staff, and external clinical partners
• Oversaw coordination of project extensions with the CRO, facilitating communication between the Singapore and US headquarters, research centres, hospitals and pharmaceutical stakeholders

Requirements:

• Bachelor’s degree in Life Sciences, Medical Sciences, or related field
• 2–5 years of experience in clinical research, clinical operations, or trial coordination
• Practical experience in site monitoringand strong understanding of ICH-GCP
• Organized, meticulous, and proactive with excellent documentation habits
• Clear communicator with the ability to work independently in a small, agile team
• Exposure to project or program management is a plus

Why Join Us

• Be part of a mission-driven biotech tackling rare diseases from Singapore
• Work in a hands-on, cross-functional environment where your contributions matter
• Competitive salary and benefits package
• Growth opportunities into clinical operations, project management, or regulatory pathways

Job Role

• The primary responsibility of this role is to manage the execution of clinical research studies.

• In addition, you will be responsible for verifying participant eligibility and obtaining informed consent prior to study enrolment.

• You will also schedule and conduct study visits in line with protocol; ensuring participant compliance and follow-up.

• Accurate and timely data collection, entry, and maintenance of tracking logs and study documentation are essential duties of this role.

• Monitoring and reporting adverse events, protocol deviations, and abnormal findings to the principal investigator (PI) and relevant authorities are critical tasks.

• Furthermore, you will coordinate and support monitoring visits, audits, and follow-up actions.

• This role requires liaison with research teams for smooth project coordination; providing regular updates and attending team meetings.

• You will also support regulatory and ethics submissions; drafting correspondence with authorities as needed.

• Study site setup, logistics, and investigator file preparation for study initiation are key responsibilities of this role.

• Last but not least, you will track study budgets and payments; managing multi-site coordination where applicable.

• Additionally, you will assist in preparing presentations, study materials, and evaluating research findings.

Key Responsibilities:

• Manage the execution of clinical research studies.

• Verify participant eligibility and obtain informed consent.

• Schedule and conduct study visits.

• Collect and maintain accurate data.

• Monitor and report adverse events.

• Coordinate monitoring visits and audits.

• Liaise with research teams.

• Support regulatory and ethics submissions.

• Track study budgets and payments.

About Us

This company aims to provide innovative solutions in clinical research. We strive to make a positive impact through our work.

Job Title: Clinical Research Coordinator #HKC

We are seeking a highly skilled and motivated Clinical Research Coordinator to join our team. The ideal candidate will have excellent organizational and communication skills, with the ability to work independently and as part of a team.

The Clinical Research Coordinator will be responsible for managing the day-to-day activities of clinical trials, including screening and recruiting participants, verifying participant eligibility, obtaining informed consent, and scheduling and conducting study visits.

• Strong organizational and time management skills
• Excellent communication and interpersonal skills
• Able to work independently and as part of a team
• Ability to maintain accurate and timely records
• Knowledge of clinical research regulations and guidelines

We offer a competitive salary and benefits package, including health insurance, paid vacation time, and opportunities for professional growth and development.

If you are a motivated and organized individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.

National Cancer Centre of Singapore Pte Ltd
Clinical Research Coordinator (Heamatology Trials)
Job Category: Research
Posting Date: 25 Mar 2025
The Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Operations’ Standard Operating Procedures.
Key Responsibilities:
Accomplish the study’s target enrolment as per agreed study timelines or shorter through effective recruitment strategies.
Regular discussion or follow-up with study team on subject screening & recruitment rates eg. email communication or team meetings with Drs.
Timely response/followup to email enquiries within 10 working days or less.
Foster good working relationships and collaborate effectively across all streams to promote operational efficiency.
Invoicing is carried out on time and payment can be received with minimal delays.
Key Requirements:
Degree in Nursing, Degree in Medicine, Pharmacy or Healthcare / biological sciences, preferably with experience in clinical trials or clinical research.
1-2 years experience in the conduct of clinical trials, specializing in Heamatology / Oncology interventional trials, governed under Health Product Act.
Must have knowledge of setting up cell therapy trials.
Must already been trained in ICH GCP.
Meticulous and possesses good organizational and time management skills.
Good communication and interpersonal skills.
Independent learner and team player who works well with external collaborators and partners.
Proactive in learning and helping other CRCs in issues with trial management.
#J-18808-Ljbffr

The Associate Clinical Research Coordinator provides research support service for clinical or

health services research, in accordance with applicable regulatory, Good Clinical Practice and

protocol requirements. He/she works closely with the Principal Investigator (PI), members of the

department, study sponsors and monitors, etc. to support and provide guidance on the

administration of the compliance, financial, personnel and other related aspects of the clinical

studies.

Responsibilities

• Act as a liaison between study participants and the research team; provide study participants with clear explanation of purpose of study and assist with obtaining informed consent
• Schedule participants for visits to clinic for the required tests and evaluations, collect their samples and assist in monitoring the participants' well-being
• Assist with compilation and management of patient data; ensure study is conducted in compliance with study protocols, established procedures and timeline
• Draft reports for submission to the relevant authorities
• Tabulate and document financial payments received or made to the study
• Other ad hoc duties as assigned

Job Requirements:

• Diploma/Adv Diploma in Nursing (on project basis), Diploma in Life Science/Pharmaceutical Science/ Clinical Trial Management
• Knowledge of MS Office software

Company description:

SingHealth Polyclinics, a leader in family medicine, provides seamless, patient-centred and preventive healthcare that is affordable and accessible to all. SingHealth Polyclinics' network of polyclinics provides primary healthcare services to the community. It plays an integral role in promoting a healthy lifestyle within the community and empowering families with the knowledge of common health issues, care and treatment options. SingHealth Polyclinics is a member of Singapore Health Services (SingHealth) - a public healthcare cluster which also manages three hospitals and five specialty centres.

Job description:

Job Description

You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.

Requirements:

• Life Science or Nursing Degree holder. Candidates with Nursing Diploma must have minimum 2 years of relevant experience
• At least 1-2 years of experience in clinical research coordination
• Ability to converse in mainstream languages (able to speak in local dialects will be an added advantage) to handle patient queries on the research study
• Strong organizational skills, able to work independently and/or a team player, meticulous in details
• Proficient with MS Office applications

You will be part of the research team involved in various clinical projects and will be required to perform the following:

• Act as a liaison between study participants and the research team; provide study participants with clear explanation of purpose of study and assist with obtaining informed consent

• Schedule participants for visits to clinic for the required tests and evaluations, collect their samples and assist in monitoring the participants' well-being

• Assist with compilation and management of patient data; ensure study is conducted in compliance with study protocols, established procedures and timeline

• Draft reports for submission to the relevant authorities

• Tabulate and document financial payments received or made to the study

Job Requirements:

• Bachelor's Degree in Nursing/ Medical Technology / Health Science / Life Science / Pharmacy
• Proficient in Microsoft Office Applications