Senior Clinical Research Associate – CNS

This is a fully remote position, open to applicants in Nevada.

📋 Description

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

• Identify and evaluate potential sites for participation in research projects.

• Execute study start-up tasks, including the collection of regulatory documentation.

• Assist in the negotiation of contracts and budget agreements.

• Provide training to sites on proper data collection methods and reporting of safety-related incidents.

• Manage site activities throughout the duration of the study.

• Conclude research activities at sites following the completion of the study.

• Conduct study initiation visits (SIVs).

• Ensure adherence to informed-consent procedures, safety-event reporting, and relevant regulatory standards.

• Travel regionally as needed.

⛳️ Requirements

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

• Outstanding organizational abilities with a keen eye for 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 CNS/Neurology is necessary.

• Must be based in the Central United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and access to in-house CRAs.

• Regular check-ins and coaching discussions with the Line Manager.

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

• Collaborative and team-focused work environment.

• Competitive benefits package based on location.

• Clear and equitable compensation structure.