Senior Clinical Research Associate – CNS/Psychiatry

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

📋 Description

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

• Engage in all phases of clinical trials, including the identification of potential sites.

• Carry out study start-up tasks, gather regulatory documentation, and assist with contract and budget discussions.

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

• Supervise site activities throughout the duration of the study.

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

• Conduct study initiation visits (SIVs).

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

⛳️ Requirements

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

• Outstanding organizational skills with a strong focus on detail.

• Capability to work independently with minimal supervision.

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

• More than 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or Nursing degree required.

• Experience in CNS/Neurology and/or Psychiatry is mandatory.

• Candidates must be located in the Central United States.

• Readiness to travel regionally is essential.

🏝️ Benefits

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

• Regular interactions and coaching discussions with the Line Manager.

• Defined career trajectory and professional growth opportunities that may lead to Clinical Trial Manager positions.

• Direct access to the Executive Leadership team.

• Competitive benefits package based on location.