Senior Clinical Research Associate – Oncology

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

📋 Description

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

• Identify and evaluate potential sites for participation in clinical research.

• Execute study start-up tasks, including the collection of regulatory documents and facilitating contract and budget discussions.

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

• Supervise site activities 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.

⛳️ 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.

• 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 residing in the United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

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

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

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

• Direct access to the Executive Leadership team.

• Competitive benefits package based on location.

• Commitment to an inclusive and equitable workplace.

• Transparent compensation structure and pay equity.