About this role
Worldwide Clinical Trials is seeking a Senior Clinical Research Associate - Oncology for a remote position based in Ontario, Canada. This full-time role supports our global, midsize CRO with a focus on advancing oncology research. You will work with diverse teams across therapeutic areas and play a key role in managing site activities, ensuring quality and compliance, and supporting study execution within a collaborative, supportive environment.
Responsibilities
- Manage the research activities at clinical sites participating in Worldwide’s trials.
- Involve yourself in all stages of the clinical study, including identifying potential sites, conducting study start-up activities, collecting regulatory documents, supporting contract and budget negotiations, training sites to collect data accurately, and reporting safety events.
- Oversee site maintenance activities and closeout of research at sites after study completion.
- Conduct study initiation visits (SIVs).
- Ensure compliance with informed consent, safety reporting, and all applicable regulatory requirements, with most site management performed remotely.
Requirements
- Excellent interpersonal, written, and verbal communication skills in English.
- Superior organizational skills with strong attention to detail.
- Ability to work with little or no supervision.
- Proficiency in Microsoft Office, CTMS, and electronic data capture (EDC) systems.
- 5+ years of experience as a Clinical Research Associate.
- A 4-year university degree or a nursing degree.
- Oncology experience is required.
- Candidate must reside in Canada.
- Willingness to travel regionally.