Senior Clinical Research Associate – Oncology

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

📋 Description

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

• Engage in all phases of clinical trials, including the selection of potential sites.

• Execute study initiation tasks, such as gathering regulatory documents and facilitating contract and budget discussions.

• Instruct sites on proper data collection procedures and the reporting of any 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 during remote site management.

⛳️ 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.

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

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

• Bachelor’s degree or Nursing degree required.

• Experience in Oncology is mandatory.

• Candidates must be located on the East Coast of the United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

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

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

• Defined career trajectory and professional growth opportunities that may lead to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package based on location.