Clinical Trials Research Assistant

Alliance For MultiSpecialty Research; Fort Myers (FL); On-site; USD 42,000 - 60,000; Full time

Job summary

Alliance For MultiSpecialty Research in Fort Myers, FL seeks a Research Assistant to support administrative and clinical tasks across studies, ensuring protocol adherence and smooth clinic flow.

Responsibilities include processing data, coordinating visits, tracking supplies, and maintaining compliant documentation while following FDA, IRB, and sponsor requirements. This role may require weekend/overtime and on-site presence.

Qualifications

• Medical office experience or equivalent work experience.
• Phlebotomy skills preferred.
• Excellent attention to detail.
• Strong listening, verbal and written communication skills.
• Excellent task management and organizational skills.
• Ability to multi-task in an evolving fast-paced environment.
• Proficient knowledge of operating office equipment and software.
• Ambulatory workday capability.
• Ability to lift/transfer/push/manipulate equipment and patients.

Responsibilities

• Prioritize tasks and meet deadlines in a fast-paced environment.
• Monitor & report adverse events, protocol deviations and safety concerns per FDA, IRB and sponsor requirements.
• Ensure compliance with study protocols, GCP and regulatory guidelines.
• Assist in subject retention efforts and engagement to support compliance.
• Perform inventory management of study supplies and lab kits.
• Maintain accurate, timely, and audit-ready documentation.
• Carry out laboratory responsibilities with proper labeling, storage and shipment of specimens.

Skills

Medical office

Phlebotomy

Attention to detail

Communication

Task management

Organizational skills

Multi-tasking

Office equipment

Education

Medical certificate

Job description

Alliance For MultiSpecialty Research in Fort Myers, FL seeks a Research Assistant to support administrative and clinical tasks across studies, ensuring protocol adherence and smooth clinic flow.

Responsibilities include processing data, coordinating visits, tracking supplies, and maintaining compliant documentation while following FDA, IRB, and sponsor requirements. This role may require weekend/overtime and on-site presence.