187 Clinical Coordinator jobs in Singapore

Location: West/ Central
Salary: Up to $3,400/month
Duration: Project basis - 6 months (renewable)
Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM

Job scope:
- Recruit and screen patients based on study eligibility, explaining study goals clearly.
- Obtain consent, administer questionnaires, and follow up with participants.
- Coordinate closely with research teams, clinicians, and clinic staff to meet study needs.
- Manage tight deadlines and achieve research targets.
- Conduct patient recruitment, data collection, and data management.
- Use databases like Redcap and hospital systems to keep accurate records.
- Ensure strict compliance with research protocols and regulations.
- Work with investigators and labs to set up clinical workflows for recruitment.
- Prepare documents for audits and assist with IRB submissions and reports.
- Maintain professional standards and adhere to hospital policies and ethics.
- Perform other related duties as assigned by the Principal Investigator (PI).

Job Requirements:
- Min. Degree in Science/ Public Health/ Social Science or any relevant field
- Adaptable, strong communication and interpersonal skills
- No experience as training will be provided

For interested applicants, please send your updated resume to:
All candidates' information will be treated with the strictest confidence
Melissa Zhang Zhiqi (Mezzo)
R
Recruit Express Pte Ltd
99C4599

Location: West/ Central
Salary: Up to $3,400/month
Duration: Project basis - 6 months (renewable)
Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM

Job scope:
- Recruit and screen patients based on study eligibility, explaining study goals clearly.
- Obtain consent, administer questionnaires, and follow up with participants.
- Coordinate closely with research teams, clinicians, and clinic staff to meet study needs.
- Manage tight deadlines and achieve research targets.
- Conduct patient recruitment, data collection, and data management.
- Use databases like Redcap and hospital systems to keep accurate records.
- Ensure strict compliance with research protocols and regulations.
- Work with investigators and labs to set up clinical workflows for recruitment.
- Prepare documents for audits and assist with IRB submissions and reports.
- Maintain professional standards and adhere to hospital policies and ethics.
- Perform other related duties as assigned by the Principal Investigator (PI).

Job Requirements:
- Min. Degree in Science/ Public Health/ Social Science or any relevant field
- Adaptable, strong communication and interpersonal skills
- No experience as training will be provided

For interested applicants, please send your updated resume to:
All candidates' information will be treated with the strictest confidence
Melissa Zhang Zhiqi (Mezzo)
R
Recruit Express Pte Ltd
99C4599

Location: West/ Central

Salary: Up to $3,500/month

Duration: Project basis - 6 months (renewable)

Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM

Job scope:

- Recruit and screen patients based on study eligibility, explaining study goals clearly.

- Obtain consent, administer questionnaires, and follow up with participants.

- Coordinate closely with research teams, clinicians, and clinic staff to meet study needs.

- Manage tight deadlines and achieve research targets.

- Conduct patient recruitment, data collection, and data management.

- Use databases like Redcap and hospital systems to keep accurate records.

- Ensure strict compliance with research protocols and regulations.

- Work with investigators and labs to set up clinical workflows for recruitment.

- Prepare documents for audits and assist with IRB submissions and reports.

- Maintain professional standards and adhere to hospital policies and ethics.

- Perform other related duties as assigned by the Principal Investigator (PI).

Job Requirements:

- Min. Degree in Science/ Public Health/ Social Science or any relevant field

- Adaptable, strong communication and interpersonal skills

- No experience as training will be provided

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

For interested applicants, please send your updated resume to:

All candidates' information will be treated with the strictest confidence

Melissa Zhang Zhiqi (Mezzo)

R

Recruit Express Pte Ltd

99C4599

Job Overview:

Clinical research coordinators play a crucial role in the success of clinical trials. As a clinical research coordinator, you will be responsible for ensuring that all research procedures are conducted in accordance with Good Clinical Practice (GCP) guidelines and institutional review board (IRB) regulations.

Key Responsibilities:

• Liaising with principal investigators and site-principal investigators to ensure smooth trial conduct
• Screening and recruiting suitable candidates as research participants
• Explain protocols to participants and collect data
• Maintaining accurate and up-to-date documentation
• Identifying and submitting protocol deviations
• Collaborating with IT specialists on data extraction

Requirements:

To be successful in this role, you will need to have a minimum diploma in biomedical science or equivalent experience. Additionally, proficiency in machine learning, cell culture, psychology, data analysis, clinical research, medicine, recruiting, protocol, data mining, Python, molecular biology, screening, medical records, and laboratory procedures is highly desirable.

Benefits:

This role offers the opportunity to work independently and as part of a team, develop strong communication and organizational skills, and gain valuable experience in clinical research coordination.

What We Offer:

A dynamic and supportive work environment, opportunities for professional growth and development, and a competitive compensation package.

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to 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 organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
• Tracking of trial expenditures and timely invoicing.

Requirements:

• 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

You will serve as part of the research team involved in clinical qualitative and/or quantitative research. Your job scopes include patient education, taking consent, performing interviews, evaluation and investigations; recording findings, maintaining equipment, optimising resources, scheduling appointments, preparing set-up and equipment; planning, co-ordinating and liaising with study participants and research team; reviewing, compiling, filing and sending data or reports; monitoring progress of study, updating and maintaining records and documentation; ensuring compliance to study protocols, established procedures and timelines.

Job requirements:

• Degree / Diploma in physiotherapy or relevant academic certification.
• A minimum of 2 years working experience is required for Diploma-holders.
• Knowledge of MS Office software.
• Experience in qualitative transcription and conducting qualitative interview preferred.

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Responsibilities:
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.
Requirements:
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.
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As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to 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 organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
Tracking of trial expenditures and timely invoicing.
Requirements:
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
#J-18808-Ljbffr

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.
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.
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