Senior Clinical Research Associate – CNS/Psychiatry

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

📋 Description

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

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

• Execute study initiation tasks, which involve gathering regulatory documents and aiding in contract and budget negotiations.

• 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, safety-event reporting, and relevant regulatory standards while managing sites remotely.

⛳️ Requirements

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

• Exceptional organizational skills with a keen eye for detail.

• Capacity to work independently with minimal supervision.

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

• At least 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 based in the Southeast.

• Willingness to travel regionally is essential.

🏝️ Benefits

• Competitive benefits package based on location.

• Support for professional development through regular check-ins and coaching sessions with the Line Manager.

• Clearly defined career progression that can lead to Clinical Trial Manager positions.

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

• Accessible Executive Leadership team.

• Commitment to an inclusive and equitable work environment.

• Transparent compensation and commitment to pay equity.