My client is a Hospital located at the Central area.
Clinical Research Coordinator - Well Clinic
1 Year Contract - 21 hours per week
Job Responsibilities
As 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.
Requirements
- 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.
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