Senior Clinical Research Associate – CNS

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

📋 Description

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

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

• Execute study start-up tasks, which include gathering regulatory documents from sites.

• Assist in the negotiation of contracts and budget agreements.

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

• Supervise site operations throughout the duration of the study.

• Conclude research activities at sites upon the completion of studies.

• Conduct study initiation visits (SIVs) to ensure readiness.

• Guarantee adherence to informed consent protocols, safety-event reporting, and relevant regulatory standards.

⛳️ Requirements

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

• Strong organizational abilities with a keen attention to detail.

• Capability 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 is highly preferred.

• Candidates must be based on the West Coast.

• Willingness to travel regionally is necessary.

🏝️ Benefits

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

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

• Clear career advancement opportunities and professional development leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package based on location.

• Transparent compensation structure and pay equity.