754 Clinical Research Associates 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

Major Duties and Responsibilities

• Liaison person 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 International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP) and Human Biomedical Research Act (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 accordance 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

1. Perform quality checks on studies as Institution Monitor (where applicable)
2. 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

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

Press Tab to Move to Skip to Content Link

Select how often (in days) to receive an alert:

• 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.

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.

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

Responsibilities:

You will assist the Director Research to develop and implement the tele-dentistry supported community-based oral care programme for seniors which includes:

·    Key conduit between National Dental Centre Singapore (NDCS), Ministry of Health, SingHealth Regional Health System (RHS), Agencies, community partners.

·    Prepare documents for and facilitate regulatory (e.g. Institution Review Board, Health Sciences Authority) approvals.

·    Facilitate the signing of project agreements with external collaborators.

·    Provide advice on programme implementation and workflow.

·    Facilitate programme-related outreach events and training sessions.

·    Design and develop informed consent form, data collection forms, logs and other study related document.

·    Execute the approved clinical research protocols in accordance to the ICH-Guideline for Good Clinical Practice (ICH-GCP), Human Biomedical Research Act (HBRA) and other regulatory requirements, including (but not limited to) assisting the principal investigator(s) in:

o   Subject's consent taking

o   Scheduling study-related appointments for research subjects

o   Completing data collection forms

o   Conducting surveys or questionnaires

o   Managing the study-related equipment

o   Handling queries by research subjects

·    Set up and maintain Investigator study file(s), including records of all approvals and reports.

·    Coordinate and take minutes for study specific meetings between the various stakeholders such as NDCS, RHS and community partners.

·    Set up and entry of research data into the study database.

·    Simple interim analysis of data.

·    Prepare study progress reports and study audits by relevant regulatory authorities and grant funding bodies.

Requirements:

·    Degree in Nursing, Biological Science, Pharmacy or other healthcare related discipline.

·    Familiar with Singapore Guideline for Good Clinical Practice (SGGCP), ethics and regulatory requirements for conducting clinical research

·    Advanced knowledge of Microsoft Excel, and bio-statistical software applications.

·    Excellent interpersonal and communication skills

·    Strong verbal and written communication skills

·    Able to work independently

·    Able to adapt in a fast-paced environment

Job Scope

• Subject recruitment & follow-up (screening, consent taking, data entry)
• Work closely with doctors, nurses & research team
• Maintain research records, support IRB applications & audits
• Ensure compliance with research protocols (HBRA, GCP)

Requirements

• Min Degree in Science / Public Health / Social Science
• Willing to travel between hospitals / sites

All Interested candidates are invited to email your resume in MS Word format to:

Please include your full working experience, education background, notice period, expected salary.

Nerissa Goh Jia Ying (R

Recruit Express Pte Ltd

Company Reg. No W | EA License Number: 99C4599

Recruiter's ref code: #HGN

We regret to inform that only suitable candidates will be shortlisted for an interview.