Senior Clinical Research Associate – CNS

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

📋 Description

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

• Identify potential locations for participation in research projects.

• Execute study start-up tasks, including the collection of regulatory documents from sites.

• Assist in negotiating contracts and budget agreements.

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

• Manage site operations throughout the duration of the study.

• Conclude research activities 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.

• Carry out the majority of site management tasks remotely.

⛳️ Requirements

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

• Strong organizational abilities with a keen eye for 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.

• Experience in the Central Nervous System (CNS) field is required.

• A bachelor’s degree or a nursing degree.

• Candidates must be residing in the United States.

• Willingness to travel within the region is a must.

🏝️ Benefits

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

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

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

• Access to the Executive Leadership team.

• Competitive benefits package that varies by location.

• A workplace that values inclusivity and equity.

• Equal employment opportunities for all candidates.