Senior Clinical Research Associate – Oncology

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

📋 Description

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

• Identify potential research sites for participation in various studies.

• Execute study initiation tasks, which include gathering regulatory documents from participating sites.

• Assist in the negotiation of contracts and budget agreements.

• Provide training to sites on proper data collection 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.

• Collaborate with colleagues across various therapeutic fields in a supportive, team-oriented setting.

⛳️ Requirements

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

• Outstanding organizational skills with a keen eye for detail.

• Capability to work independently with minimal supervision.

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

• A minimum of 5 years of experience as a Clinical Research Associate.

• A bachelor’s degree or a Nursing degree is required.

• Experience in Oncology is mandatory.

• Candidates must be residents of the East Coast.

• Willingness to travel regionally is required.

🏝️ Benefits

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

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

• Defined career advancement opportunities and professional development pathways leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package tailored to location.