Senior Clinical Research Associate – Oncology

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

📋 Description

• Oversee research activities at locations involved in Worldwide’s clinical research initiatives.

• Identify and evaluate potential sites for research participation.

• Execute study start-up tasks, including the collection of regulatory documents from participating sites.

• Assist in the negotiation of contracts and budgets.

• Provide training to sites for accurate data collection and reporting of safety-related incidents.

• Manage site operations throughout the study maintenance phase.

• Conclude research activities at sites following the completion of the study.

• Conduct study initiation visits (SIVs).

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

⛳️ 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.

• 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 residents of the Central 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 professional development opportunities leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package based on location.