Senior Clinical Research Associate – Oncology

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 prospective sites for participation in clinical studies.

• Execute study initiation tasks, which include gathering regulatory documents and assisting in contract and budget discussions.

• Educate sites to accurately collect data and report any potential safety-related incidents.

• Supervise site operations throughout the maintenance phase of the study.

• Conclude research activities at locations once studies are completed.

• Conduct study initiation visits (SIVs).

• Ensure adherence to informed-consent protocols, safety-event reporting, and relevant regulatory standards.

• Carry out most site-management responsibilities remotely.

⛳️ Requirements

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

• Outstanding 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.

• Bachelor’s degree or Nursing degree required.

• Current experience in Oncology is necessary.

• CAR-T experience is preferred.

• Proficiency in both written and spoken English is a must.

• Applicants must reside within the contiguous United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

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

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

• Clearly defined career progression and professional development opportunities that may lead to Clinical Trial Manager positions.

• Accessible Executive Leadership team.

• Competitive benefits package based on location.