Research Assistant
On-siteDoral, Florida, United States
Job Summary
Prioritize administrative and clinical tasks to ensure study completion per protocol while maintaining strict compliance with FDA, IRB, and GCP regulations. Monitor and report adverse events, protocol deviations, and serious adverse events, ensuring accurate documentation of vital signs, EKGs, and specimen handling. Manage subject retention through engagement and interviews, perform phlebotomy, and handle inventory for lab kits and investigational products. Assist monitors during onsite visits, screen subjects, prepare consents, and maintain audit-ready logs for enrollment and informed consent. Work in a fast-paced environment requiring strong problem-solving skills, attention to detail, and the ability to handle confidential information with discretion. Occasional weekend and overtime hours may be required.
Required Qualifications
- Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination
- Ability to be ambulatory most of the workday
- Position may require occasional weekend and/or overtime hours
- Fluent in English
- Classification: Non-Exempt
Desired Qualifications
- Medical office experience, medical certificate, or equivalent work experience preferred
- Phlebotomy skills are preferred
- Excellent attention to detail
- Strong listening, verbal and written communication skills
- Excellent task management and organizational skills
- Ability to multi-task in an always evolving fast paced environment
- Demonstrate proficient knowledge of operating office equipment and software
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