Senior Clinical Research Associate – Psychiatry

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

📋 Description

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

• Engage in all phases of clinical studies, which includes identifying potential research sites.

• Execute study start-up tasks, such as gathering regulatory documents and aiding in contract and budget discussions.

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

• Supervise site activities throughout the study maintenance period.

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

• Conduct study initiation visits (SIVs).

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

• Travel regionally as needed.

⛳️ Requirements

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

• Outstanding organizational abilities with a keen attention to detail.

• Capability to work independently with minimal supervision.

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

• Over 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or Nursing degree.

• Experience in Psychiatry is mandatory.

• Must be a resident of the Southeastern United States.

• Willingness to travel regionally is required.

🏝️ Benefits

• Competitive benefits package tailored to location.

• Professional development opportunities through regular check-ins and coaching sessions with the Line Manager.

• Defined career trajectory and growth that can lead to Clinical Trial Manager positions.

• Assistance with regulatory submissions, TMF management, and in-house CRAs for projects that require intensive site management.

• Access to the Executive Leadership team.

• An inclusive and equitable workplace environment.

• Transparent compensation structure and pay equity.