Clinical Research Coordinator (medellin, Colombia)
IQVIA
Bogota, Colombia
Perform clinical procedures
Collect and record data
Patient recruitment and screening
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies
Job Summary
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies.
Provide clinical research support to investigators to prepare for and execute assigned research studies, including reviewing study protocols and collecting regulatory documentation.
Assist research site with coverage planning related to staffing and scheduling for research projects and prepare for study monitoring visits, audits, and regulatory inspections.
Matching Summary
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies.
Skills & Requirements
Must-have
perform clinical procedures
collect and record data
patient recruitment and screening
manage study visits and procedures
handle lab testing and logistics
monitor subject safety
data quality checking and resolution
Nice-to-have
excellent interpersonal skills
attention to detail
effective working relationships
training new staff members
Key Requirements
Bachelor's Degree in Life Sciences or Health Care
3 years' relevant work experience
Working knowledge of clinical trials
Working knowledge of GCP principles
Skill in carrying out required clinical procedures
Good skill in using MS Windows and Office applications