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Johnson & Johnson Innovative Medicine
Overview
Develops and coordinates clinical and regulatory documents, including protocols and clinical study reports, within the oncology therapeutic area. Collaborates with cross-functional teams to establish document timelines and ensure adherence to internal standards and regulatory guidelines.
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Compensation
CA$74,000 - CA$119,600 / YEAR
Posted
4 days ago
ICON plc
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Salary not listed
8 days ago
Everest Clinical Research
The Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
CA$65,000 - CA$100,000 / YEAR
4 months ago
