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.

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.