1,308 Clinical Positions jobs in Singapore

Overview

Associate Clinical Research Coordinator / Clinical Research Coordinator role at Singapore General Hospital.

Responsibilities

• Provide research support service for clinical research in accordance with applicable regulatory, Good Clinical Practice (GCP) and protocol requirements.
• Work closely with Principal Investigators (PIs) to assist with organisation of study initiation meetings, IRB submissions, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.
• Support SGH's mission of providing quality patient care, education and research.

Qualifications

• 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
• Excellent interpersonal skills

Employment type

• Full-time

Seniority level

• Entry level

Job function

• Research, Analyst, and Information Technology

Industries

• Hospitals and Health Care

We are looking for a candidate who will be assisting investigators in conducting clinical trial s 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.

Key Responsibilities:

• 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.

Requirements :

• 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.

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.

1 day ago Be among the first 25 applicants

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance with 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 with their treatment and follow-up
• Data collection and management including resolving data discrepancies
• Coordinating the collection of biological specimens
• Monitoring 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

• Degree in Life Sciences/Nursing
• OR Diploma in Nursing with minimum 6 years of working experience as CRC
• 2 years of related working experience will be advantageous
• Excellent time-management and communication skills
• Able to work independently and as a team
• Detail-oriented and self-motivated
• Good grasp of MS Office applications

• Mid-Senior level

• Full-time

The Project Coordinator will provide project management, support and coordination of programmatic activities and contribute to patient engagement activities and clinical research support in the healthcare sector. The role will strengthen patient and stakeholder relationships and will work with internal and external stakeholders as an integral member of the team.

• Calls patient to confirm and update patient details.
• Elaborate work reports according to the projects' guidelines.
• Monitor project schedule, escalate discrepancies and support issue resolution.
• Develop and implement patient support program and scheduling procedures and process improvements.
• Complying with data protection law, including responding promptly to queries
• Update and maintain internal databases, tracking systems and project plans.
• Prepare presentation materials for meetings and project summary data.
• Provide project management and operational support as directed by stakeholders.

• Bachelor’s Degree or equivalent studies in Pharmacy, Nursing, Life Sciences
• Excellent communication, organizational and interpersonal skills
• Written and verbal communication skills
• Fully competent in Microsoft Office programs and strong with Excel
• Effectively and efficiently manage multiple tasks
• Enthusiastic, projects a positive attitude, and easily adapts to change

• Entry level

• Full-time

• Project Management and Information Technology

• Hospitals and Health Care

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

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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.

• Liaise with PI and site-PI to ensure effective communication and coordination.
• Manage and maintain accurate records and documentation.
• Screen and recruit suitable candidates according to protocol requirements.
• Explain protocols to participants and obtain informed consent.
• Coordinate appointments and schedule within specified timeframes.
• Perform research procedures and collect data accurately.
• Maintain source documentation and patient reimbursement logs.
• Identify and document protocol deviations and submit to Institutional Review Board.
• Communicate adjustments and changes to PIs and collaborators.
• Report and follow up on unanticipated problems and adverse events.

• Minimum Diploma in Biomedical Science or equivalent.
• Experience as a Research Assistant preferred.