Offer summary
Qualifications:
College or university degree in Life Science, Prior experience in coordinating clinical trials, Ability to work in fast-paced environment.Key responsabilities:
- Act as main communication line between Sponsor/CRO and site
- Ensure timely response to feasibility questions
- Track patient enrollment, support meeting project timelines
- Accurate data entry into study specific EDC systems
- Prepare for and participate in onsite audits or inspections