Senior Clinical Research Associate – CNS/Psychiatry

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

📋 Description

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

• Engage in all phases of clinical studies, including identifying suitable sites.

• Execute study start-up tasks, which involve gathering regulatory documents and assisting in contract and budget negotiations.

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

• Supervise site activities throughout the study maintenance phase.

• Conclude research operations at sites post-study completion.

• Perform study initiation visits (SIVs).

• Ensure adherence to informed-consent protocols, safety-event reporting, and relevant regulatory standards, primarily through remote management of sites.

⛳️ 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.

• A 4-year university degree or a Nursing Degree.

• Required experience in CNS/Neurology and/or Psychiatry.

• Candidates must be residents of the Northeast.

• Willingness to travel regionally is essential.

🏝️ Benefits

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

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

• Clearly defined career trajectory and professional growth opportunities leading to Clinical Trial Manager positions.

• Direct access to the Executive Leadership team.

• Competitive benefits package tailored to location.