Résultats de recherche

Parexel is looking for a Medical Director with a very strong background in Ophthalmology to join our Global Medical Sciences team. Parexel is in the business of improving the world’s health. The ability to travel 15% domestically or internationally is required.

A global biopharmaceutical services company is looking for a Medical Director with substantial experience in Ophthalmology to contribute to clinical oversight and client engagement in Canada.The role is remote and involves vital responsibilities, including medical monitoring, client relationship man

A global biopharmaceutical services company is looking for a Medical Director with substantial experience in Ophthalmology to contribute to clinical oversight and client engagement in Canada.The role is remote and involves vital responsibilities, including medical monitoring, client relationship man

Parexel is looking for a Medical Director with a very strong background in Ophthalmology to join our Global Medical Sciences team. Parexel is in the business of improving the world’s health. The ability to travel 15% domestically or internationally is required.

A global biopharmaceutical services company is looking for a Medical Director with substantial experience in Ophthalmology to contribute to clinical oversight and client engagement in Canada.The role is remote and involves vital responsibilities, including medical monitoring, client relationship man

Serve as the Document Specialist representative on assigned project, with departmental supervision: communicate requirements, conduct team review of draft and final documents, attend study team meetings to agree on expectations, inform about the timeline, and advance document publishing to approval,

A global clinical research organization seeks a Senior Clinical Research Associate responsible for managing and monitoring clinical trial sites.This role demands at least 3 years of site monitoring experience, preferably in Oncology, as well as a strong understanding of clinical trial methodologies

The Senior Clinical Research Associate (Sr.CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and

A leading global clinical research organization is currently seeking a highly motivated Regulatory Affairs professional to join their team in Canada.As a Senior Regulatory Affairs Associate, you will act as the primary contact with health authorities, ensuring compliance with Health Canada regulatio

Bring your expert knowledge of Health Canada regulatory requirements and guidelines to Parexel!. We are currently seeking a highly motivated Regulatory Affairs professional to join Parexel and contribute their knowledge of Health Canada regulatory requirements and processes to a major, dedicated cli