Senior Clinical Research Associate – Oncology

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

📋 Description

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

• Identify potential sites for participation in clinical research.

• Execute study start-up tasks, which include gathering regulatory documents and facilitating contract and budget negotiations.

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

• Manage site operations during the maintenance phase of studies.

• Conclude research activities at sites upon study completion.

• Conduct study initiation visits (SIVs).

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

• Collaborate with colleagues across various therapeutic areas and specialties.

⛳️ 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 is required.

• Experience in Oncology is mandatory.

• Candidates must be residents of Canada.

• Willingness to travel regionally is necessary.

🏝️ Benefits

• Comprehensive support through regulatory submissions, TMF management, and in-house CRAs.

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

• Defined career progression and professional development opportunities leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• A diverse and inclusive workplace culture.

• Equal employment opportunities for all.

• Exceptional employee experience.