Senior Clinical Research Associate

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

📋 Description

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

• Involve yourself in every phase of clinical studies, encompassing site identification, study initiation, regulatory document gathering, support for contract and budget negotiations, site training, study management, and site closure.

• Execute study initiation visits (SIVs).

• Conduct the majority of site management tasks remotely.

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

⛳️ Requirements

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

• Outstanding organizational capabilities with a keen eye for detail.

• Capacity to operate with minimal or no supervision.

• Proficiency in Microsoft Office, CTMS, and EDC Systems.

• A minimum of 5 years of experience as a Clinical Research Associate, OR a 4-year university degree, OR a Nursing Degree.

• Experience in Oncology, CNS, or Rare Disease is mandatory.

• Applicants must reside in Canada.

• Availability for regional travel is required.

• Bilingual proficiency in French and English.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and in-house CRAs for projects that demand extensive site management.

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

• Well-defined career trajectory and professional growth opportunities leading to Clinical Trial Manager positions.

• Accessible Executive Leadership team.

• Equal employment opportunities and a diverse, inclusive workplace.