1,781 Clinical Positions jobs in Singapore

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

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Associate Clinical Research Coordinator / Clinical Research Coordinator
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:
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 skills
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Our client in the healthcare industry is looking to hire Clinical Research Coordinators (CRC) to assist in a Human Biomedical Research study. As a CRC, you will be primarily responsible for subject recruitment and other research deliverables for the studies, and work closely with the research team and Principal Investigator.

• Be involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms
• Obtain consent taking, administer study questionnaires and follow-up on study participants.
• Work closely with research team, clinicians, clinic staff and other relevant internal departments to ensure research study needs are met.
• Able to work on tight timelines, set sensible targets and achieve research deliverables.

• Conduct research study activities like patient recruitment, data collection and data management.
• Assist in data collection from electronic health records.
• Set up and maintain study investigator files, including records of consent taken and blood collection.
• Maintain study records in databases such as Redcap and in electronic health record systems.
• Responsible for maintaining strict adherence to research protocols i.e., HBRA.
• Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.
• Prepare necessary documentation for audit purposes.
• Coordinate the submission of new IRB applications, study amendments and annual reports.
• Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.
• Assist with any other duties of a similar nature that are delegated by the PI.

• Bachelor Degree in Science/ Public Health/ Social Science with 2 years relevant experience
• Fresh graduates are welcome to apply.
• Able to adapt in a fast-paced environment, with a strong focus to meet research deliverables and targets.
• Strong interpersonal and communication skills. Leadership and accountability to tasks is very desirable.
• Independent and mature. Able to work independently, as well as in a team.
• Meticulous, well-organized and able to multi-task
• Ability to work in an interdisciplinary environment with different groups of stakeholders.
• Bilingual preferred (fluent in Mandarin/Malay/Tamil).
• Willing to travel between the Hospitals and external study sites as part of his / her work.
• Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM, are required.
• Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)

Interested candidates, please click “Apply Now” or send your resume to

We regret that only shortlisted candidates will be notified.

Felicia Lua Wei Xuan | CEI Reg. No.: R

Job Lions Pte Ltd | EA Licence No.: 21C0594

Overview

We are looking for a candidate who will assist investigators in conducting clinical trials and/or clinical research studies at the National Neuroscience Institute, in adherence to Good Clinical Practice (GCP) Guidelines, protocol requirements, and other applicable regulatory and ethical guidelines, SOPs and hospital policies.

• Plan, manage and conduct clinical trials from study start-up, perform study-related activities, such as screening and recruitment of study subjects; assist with obtaining informed consent; coordination of subject visits; data entry and other procedures, to study closure.
• Assist in IRB and/or regulatory application submissions.
• Collect, handle and process specimens in accordance with the protocol/lab manual.
• Take vital signs and ECG recordings.
• Maintain the Investigator Site Files and ensure all study documents are accurate, complete and up-to-date.
• Manage Investigational Products.
• Assist in adverse events reporting.
• Administer study-related questionnaires.
• Draft and manage study budgets and timelines, and prepare billing documents to sponsors.
• Conduct study monitoring visits for IITs.
• Train and mentor junior staff.
• Work closely with internal and external stakeholders to ensure all study-related activities are carried out efficiently.

• Bachelor’s degree in Life Sciences, Nursing, or related fields. Candidates with at least 4 years of clinical trial experience is preferred.
• Strong knowledge of GCP guidelines and regulatory requirements.
• Good written, communication and interpersonal skills. Ability to speak other languages will be an added advantage.
• Strong organisational, time management and problem-solving skills.
• Meticulous and able to work independently.
• Good team player.
• Proficient in Microsoft applications.
• Prior experience in monitoring would be most advantageous.

Responsibilities

• Required to assist the investigators in overall administration of clinical research activities prior to, during and post study such as enroll suitable subjects, take vital signs, collect and process biological samples,collect and enter data, monitor 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) and in compliance with the Regulations and ICH Good Clinical Practice Guideline
• Attend investigator’s meeting (local/overseas) and site initiation meeting as assigned and liaise with relevant internal and external agencies during the course of work

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

Only shortlisted candidates will be notified

Overview

Clinical Research Coordinator responsibilities and related activities at the hospital/healthcare research program.

• Liaison with Principal Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc.
• Plan, organise and coordinate the workflow of the research study
• Adhere to protocol procedure
• Screen research participants for eligibility according to research protocol
• Enrol research participants and ensure their compliance to research procedures
• Explain protocol to research participants and ensure that informed consent is taken as per ICH GCP and HBRA requirements
• Schedule appointments for research participants within the time frame required in the protocol
• Arrange for clinical/ laboratory tests and investigations; update schedule visit logs
• Draw, centrifuge blood specimens and send specimens to laboratory or store specimens in accordance with requirement of research protocol
• Assist in the completion and maintenance of biological specimen logs
• Trace and return of case notes, blood results and all other results required in the protocol
• Assess subject’s condition; coordinate physical examinations per protocol; record medical drug history according to protocol
• Collect and maintain data, as well as provide study reports
• Maintain documentation of patient reimbursement logs, hardcopy and electronic case report forms
• Maintain investigator files and source documentation for each patient according to protocol requirements
• Identify, document and submit protocol deviations to Institutional Review Board (IRB) according to research requirements
• Inform PIs, Co-Investigators, collaborators and study team members on any adjustments based on protocol change
• Complete, report and follow up on unanticipated problems involving risk to subjects and adverse events and/or serious adverse events
• Traveling to research participants’ house may be required
• Work closely with SOC clinical staff (e.g. physicians, PSAs) in clinical decision support, therapeutic interventions, and first-visit interventions

• Mentor junior clinical research staff

• Perform quality checks on studies as Institution Monitor (where applicable)
• Be a NHG Committee of Practice (CoP) or Faculty member in CRC Society (where applicable)
• Participate in projects and activities as assigned by the Team Lead or Director, Clinical Research Unit

• Executive

• Full-time

• Health Care Provider and Research

• Hospitals and Health Care

Yishun, North Region, Singapore

Overview

The purpose of this role is to provide significant technical expertise in architecture planning and design of the concerned tower (platform, database, middleware, backup etc) as well as managing its day-to-day operations.

• Provide adequate support in architecture planning, migration & installation for new projects in own tower (platform/dbase/middleware/backup)
• Lead the structural/architectural design of a platform/ middleware/ database/ back up etc. according to various system requirements to ensure a highly scalable and extensible solution
• Conduct technology capacity planning by reviewing the current and future requirements
• Utilize and leverage the new features of all underlying technologies to ensure smooth functioning of the installed databases and applications/ platforms, as applicable
• Strategize & implement disaster recovery plans and create and implement backup and recovery plans
• Manage day-to-day operations of the tower by troubleshooting issues, conducting root cause analysis (RCA) and developing fixes to avoid similar issues
• Plan for and manage upgradations, migration, maintenance, backup, installation and configuration functions for own tower
• Review the technical performance of own tower and deploy ways to improve efficiency, fine tune performance and reduce performance challenges
• Develop shift roster for the team to ensure no disruption in the tower
• Create and update SOPs, Data Responsibility Matrices, operations manuals, daily test plans, data architecture guidance etc.
• Provide weekly status reports to the client leadership team, internal stakeholders on database activities w.r.t. progress, updates, status, and next steps
• Leverage technology to develop Service Improvement Plan (SIP) through automation and other initiatives for higher efficiency and effectiveness

• Team Management: Resourcing, Talent Management, Performance Management, Employee Satisfaction and Engagement
• Resourcing: Forecast talent requirements, hire resources, train direct reportees
• Talent Management: Onboarding, training, career progression, diversity in leadership
• Performance Management: Set goals, conduct reviews, provide feedback
• Employee Satisfaction and Engagement: Lead engagement initiatives, track satisfaction, provide enriching projects
• Deliver: Align with SLA, risk mitigation, knowledge management, CSAT/Customer Experience, timely project delivery

• Mandatory Skills: Linux Admin
• Experience: 5-8 Years

Location: Not specified in the provided excerpt. Shift and schedule: Shift system. This section originally includes additional corporate boilerplate and descriptions not directly tied to a single role.

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