About this role
Responsible for the scientific integrity of the clinical program. Translates scientific information into business concepts;
Interacts with medical and scientific experts to validate scientific concepts and create product advocacy;
Leads the preparation of the scientific rationale and design of study protocol;
Follows patient safety parameters throughout the study and answers scientific and medical questions from study sites, liaising with medical director as appropriate;
Researches protocol-specific technologies;
Leads the analysis and interpretation of study results and the creation of the final study report;
Writes abstracts and manuscripts for publication;
Critically reviews scientific literature and disseminates relevant information;
Reviews the scientific accuracy of corporate materials for external use;
Prepares scientific documents, as required;
Manages the Medical Writer under his / her responsibility;
Leads key cross-functional initiatives relating to Regulatory submissions;
Acts as an internal scientific resource for more junior team members.
Good oral presentations skills;
Autonomy and initiative;
Good communication skills and team spirit;
Excellent writing skills and aptitude for creating reports;
Good planning and organizational skills;
Good people management skills;
Doctoral degree (MD, PharmD, PhD) in a medical / scientific discipline;
Experience in clinical research within the biopharmaceutical industry an important asset.
What we offer
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