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Clinical Research Coordinator
9 minutes ago
Singapore National University Hospital Full time**Job Purpose** The Clinical Research Coordinator will work closely with the Department of Anaesthesia to coordinate and ensure the smooth running of research studies within the Department. **Duties and Responsibilities** **_Primary Responsibilities and Dutiies_** - Assist with research study design, preparation of study documents - Coordinate...
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Singapore Alexandra Hospital, Singapore Full timeClinical Research Coordinator, Healthcare Redesign Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra Hospital, Singapore Clinical Research Coordinator, Healthcare Redesign 2 days ago Be among the first 25 applicants Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra...
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Singapore Alexandra Hospital, Singapore Full timeClinical Research Coordinator, Healthcare Redesign Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra Hospital, Singapore Clinical Research Coordinator, Healthcare Redesign 2 days ago Be among the first 25 applicants Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra...
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Singapore Alexandra Hospital, Singapore Full timeClinical Research Coordinator, Healthcare Redesign Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra Hospital, Singapore Clinical Research Coordinator, Healthcare Redesign 2 days ago Be among the first 25 applicants Join to apply for the Clinical Research Coordinator, Healthcare Redesign role at Alexandra...
Hospital Research Coordinator
4 weeks ago
My client is a Hospital located at the Central area.
Clinical Research Coordinator - Well Clinic
1 Year Contract - 21 hours per week
Job ResponsibilitiesAs part of the research team, you will be responsible for:
- Assisting investigators in the recruitment, screening, consent-taking, and follow-up of study participants, ensuring full compliance with the study protocol, regulatory standards, and ethical guidelines.
- Coordinating the collection and transport of biological samples, and overseeing the monitoring and reporting of adverse events and safety-related information.
- Managing study data, including accurate entry and validation, extraction of relevant information from medical records, and maintaining essential documentation such as investigator files.
- Organizing and preparing data for input into databases, ensuring accuracy and consistency to support the productivity and effectiveness of the research team.
- Identifying and resolving missing or inconsistent data and addressing discrepancies.
- Scheduling visits and coordinating logistics for study participants and stakeholders, including handling related financial matters such as reimbursements.
- Providing support for general administrative tasks or other coordination duties as required.
- A Bachelor's degree in health sciences, life sciences, nursing, or a related field; OR a Diploma in a similar field with a minimum of 3 years of experience as a Clinical Research Coordinator (CRC).
- Prior experience in clinical trials and/or project coordination within a healthcare setting is an added advantage.
- Strong time management and communication skills.
- Ability to work both independently and collaboratively as part of a team.
- Proficient in using hospital systems (e.g., NGEMR EPIC), Microsoft Office applications (Word, Excel, PowerPoint), and research platforms such as REDCap.
Microsoft Office
Clinical Research
Healthcare
Clinical Trials
Protocol
PowerPoint
Time Management
Communication Skills
Nursing
Project Coordination
Health Sciences
Life Sciences
Screening
Medical Records
Scheduling
Databases
