Senior Clinical Research Associate – Rare CNS

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

📋 Description

• Oversee research activities at sites involved in Worldwide’s clinical research initiatives.

• Identify potential sites for participation in research projects.

• Execute study start-up tasks, including the collection of regulatory documents and assisting with contract and budget negotiations.

• Train sites on proper data collection methods and the reporting of safety-related incidents.

• Manage site operations throughout the study maintenance phase.

• Conclude research activities at sites following the study's completion.

• Carry out study initiation visits (SIVs).

• Ensure adherence to informed consent protocols, safety-event reporting, and relevant regulatory requirements.

• Collaborate with team members across various therapeutic areas and specialties.

⛳️ Requirements

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

• Outstanding organizational skills with a strong attention to detail.

• Capacity to work independently with minimal supervision.

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

• A minimum of 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or Nursing Degree required.

• Experience in Rare CNS is mandatory.

• Must live in the Southeastern United States; preference given to Florida residents.

• Willingness to travel regionally is necessary.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and assistance from in-house CRAs.

• Regular check-ins and coaching sessions with your Line Manager.

• Clear career trajectory and professional growth opportunities leading to Clinical Trial Manager positions.

• Competitive benefits package based on location.

• Open and transparent compensation structure ensuring pay equity.