460 Clinical Research Associates jobs in Singapore

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

Job Responsibilities:

• 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.

Job Requirements:

• 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.

To apply for this position, please email your detailed resume, including your current and expected salary, to .

We regret to inform that only shortlisted candidates will be notified.

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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.

• 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.

• 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 organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
• Tracking of trial expenditures and timely invoicing.

• Degree in Life Sciences/Nursing
• OR Diploma in Nursing with minimum 6 years 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

• Working Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM, are required.
• Location: Queenstown

• Bachelor Degree in Science/ Public Health/ Social Science with 2 years relevant experience

Job Responsibilities:

• 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.

Job Requirements:

• 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.

To apply for this position, please email your detailed resume, including your current and expected salary, to

We regret to inform that only shortlisted candidates will be notified.

Join a leading Government Hospital with attractive benefits, including AWS, 2–3 months' performance bonus, good leave policy, and medical coverage.

Benefits:

• Government Hospital - Stable industry
• AWS + 2-3 months performance bonus + yearly salary increment
• Good leave policy + medical benefits

You will be responsible for the following:

1) Subject Recruitment and follow up

2) Research Documentation / Administrative duties

· 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.

Requirements

· Bachelor Degree in Science/ Public Health/ Social Science

· Able to adapt in a fast-paced environment.

· Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

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**We regret to inform that only shortlisted candidates would be notified.

Chanel Loh Su Fui

Registration Number: R22110419

EA License No: 06C2859 (MCI Career Services Pte Ltd)