Clinical Research Coordinator I
Core
Coordinate and manage hereditary cancer syndrome research projects, including patient identification, enrollment, data collection, and regulatory compliance for genetic testing and genomics studies.
Role type
Clinical Research Coordinator (IC)
Builds
Hereditary cancer detection studies, tumour profiling studies, and liquid biopsy research programs
Domain
Healthcare / Oncology / Clinical Research
Deliverable
client delivery
Required skills
Patient recruitment and screening, informed consent execution, data collection and entry, regulatory compliance (ICH/GCP), database maintenance, electronic patient record systems, IATA shipping regulations knowledge
Preferred skills
Clinical Research Professional certification, experience with liquid biopsy studies, knowledge of genomic technologies
Technologies
MS Office (Word, Excel, Outlook), electronic patient record systems
Responsibilities
Identify patients fulfilling hereditary genetic testing criteria, enroll patients into tumour profiling studies, coordinate liquid biopsy studies, recruit study participants, plan and implement data collection and source documentation, collaborate on participant recruitment and database updates, execute administrative tasks for regulatory submissions
Seniority
Junior to Mid-level, hands-on IC
