Senior Clinical Research Associate – Oncology

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

📋 Description

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

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

• Execute study initiation tasks, such as gathering regulatory documentation and assisting with contract and budget discussions.

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

• Supervise site activities throughout the study maintenance phase.

• 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 while managing sites remotely.

⛳️ Requirements

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

• Strong organizational abilities with a keen eye for detail.

• Capability to operate 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.

• Experience in Oncology is mandatory.

• Candidates must be located in the Midwest United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

• Competitive benefits package based on location.

• Opportunities for professional growth through regular feedback and coaching sessions with a Line Manager.

• Defined career progression leading to Clinical Trial Manager positions.

• Collaborative and supportive work environment.

• Commitment to an inclusive and equitable workplace.