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| Job #03123 |
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| About our client |
| Our client is a global CRO that serves the
pharmaceutical, biotechnology and medical device industries. They are built upon
a strong foundation of clinical, process and systems expertise. The company has
an experienced management team, a robust pipeline and an empowering corporate
culture that is focused on the professional development of its employees. |
| Position |
Location |
| Director Clinical Affairs |
British Columbia |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Manage the activities and performance of the Clinical Department 2) Generate global study protocols 3) Act as a primary contact and provide support to clinicians and patients for worldwide investigational products and product licensing 4) Ensure data collection and study protocols comply with regulatory requirements 5) Provide statistical clinical outcomes and reports that support worldwide regulatory submissions 6) Support reimbursement activities for company’s products 7) Provide and assist in regulatory compliance in the distribution and use of study and/or regulated products |
| Requirements |
1) Advanced degree in Nursing, Biomedical Engineering or a related discipline 2) 6+ years of experience in clinical supervision in biologics 3) Experience in designing and completing clinical studies 4) Expertise in the support and implementation of reimbursement strategies 5) Experience in supporting business development efforts in the company’s international offices 6) Strong knowledge of human anatomy and scientific methods 7) Excellent problem-solving and decision-making skills 8) Self-motivated with a proactive attitude and the ability to work independently 9) Willingness to travel (internationally) |

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