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gcp clinical trials ich data reporting hipaa📋 Description
- Interact with potential trial candidates via phone/email/text.
- Schedule visits and coordinate participant statuses with site staff.
- Report to assigned manager; provide recruitment support.
- Collaborate with site personnel to address questions and updates.
- Maintain regular Microsoft Teams and email communications for prompt responses.
- Establish relationships with site personnel across multiple sites.
🎯 Requirements
- Bachelor’s degree or equivalent experience.
- 2 years of experience with clinical trial sites, physicians, and/or patients.
- Clinical Trial Coordinator experience preferred, not required.
- Exceptional communication and customer service.
- Fluent in local/native language of assignment.
- Independent work ethic; strong time management.
- Confidentiality and data privacy commitment.
🎁 Benefits
- This is a freelance, hourly contract position.
- Contract pays hourly rate as agreed.
- Remote work available.
- No employee benefits or paid leave.
- Contractors provide own computer and headset.
- Invoices must follow contract terms.
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