Job Summary
You will oversee and coordinate clinical research studies, managing administrative and operational activities to ensure smooth execution and compliance. You will collaborate with multiple stakeholders to drive research outcomes and support informed consent processes.
Responsibilities
- Lead pre-study preparatory activities to ensure readiness and compliance for clinical research studies
- Coordinate participant recruitment and manage related research activities including study monitoring and maintaining accurate participant logs
- Collaborate with other study sites and research institutes to align workflows and share study progress
- Organize and streamline study workflows and assist with the subject informed consent process
- Prepare study applications, reports, and documentation to meet regulatory and institutional requirements
- Communicate effectively in writing and verbally to document study progress and collaborate with team members
- Work independently and collaboratively within cross-functional teams to achieve research objectives
- Adapt and apply resourcefulness to resolve challenges encountered during study execution
Preferred competencies and qualifications
- Bachelor's degree in sciences, Public Health, or equivalent
- Experience in clinical research is advantageous
- Able to work independently and resourceful
- Good witten and verbal communication skills
- Relevant training will be provided when necessary
