Offer summary
Qualifications:
High School Diploma/Certificate or equivalent, Bachelor’s degree preferred, Good Documentation Practices knowledge, Good Clinical Practices knowledge, At least 1 year of clinical research experience preferred.
Key responsabilities:
- Support clinical study teams at Country/Site level
- Perform quality checks prior to eTMF submissions
- Assist with resolution of QC findings for eTMF
- Prepare and distribute Investigator Site Files
- Update and maintain site level CTMS as needed