Medical Affairs

The Medical Affairs department is responsible for two functions within Roche Canada: operational aspects of post-approval clinical studies required by Roche Canada business, and provision of guidance on the Rx & D Code as followed by member companies of Rx & D, such as Roche. The clinical trial function encompasses all aspects of clinical trials, from planning, start-up, conduct and close-out. Roles in compliance and training, contract administration and systems are integral to the department. A background in medical sciences and solid experience in clinical trial conduct, including site monitoring and project management are key requirements for this function, as is the understanding and application of ICH-GCP and regulatory guidelines for the conduct of clinical trials. Experience working with Clinical Research Organizations (CROs) is an added benefit. This function requires individuals with strong communication skills, organizational abilities, attention to detail and customer focus. The Medical Affairs function related to the Rx & D Code requires a solid understanding of the Code and its application to health care professionals. This function requires strong communication skills including presentation, writing and training skills. Experience working in facets of the Code such as Continuing Health Education, are also beneficial. All of the functions within Medical Affairs operate in strong process oriented environments.