This is a fully remote position, open to applicants in Florida, +1 more state.

📋 Description

• Oversee research operations at sites involved in Worldwide's clinical research initiatives.

• Assist in all phases of clinical trials, which includes identifying sites, initiating studies, gathering regulatory documents, negotiating contracts and budgets, training sites, maintaining studies, and closing out sites.

• Perform study initiation visits (SIVs).

• Ensure adherence to informed consent protocols, safety-event reporting, and relevant regulatory standards while managing sites from a distance.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in English.

• Outstanding organizational skills with a keen eye for detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, CTMS, and EDC Systems.

• Over 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or a Nursing degree.

• Experience in CNS/Neurology is mandatory.

• Applicants must reside in the Southeast region.

• Willingness to travel locally is required.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and in-house CRAs for projects requiring extensive site management.

• Regular communication and coaching sessions with the Line Manager.

• Defined career trajectory and opportunities for professional growth toward Clinical Trial Manager positions.

• Accessible Executive Leadership team.

• Competitive benefits package based on location.