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| Job #03554 |
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| About our client |
| Our client is a large, world-class medical device company focused on cardiology therapies, among others. They offer a stable, team environment for all employees and are committed to developing each individual's skill-set. This is an excellent opportunity for the right person. |
| Position |
Location |
| Clinical Research Associate |
Quebec |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Review agreed clinical investigation plan summary and scheduling implementation. 2) Prepare patient documentation templates and tools. 3) Provide logistical and technical support as requested i.e.: center initiation activities. 4) Present study objectives to selected investigators. 5) Produce relevant documentation and expectations to selected investigators. 6) Follow up on patient recruitment progress. 7) Highlight deviations in study progress and discuss corrective action with Clinical Project Leader or Manager; communicates to study sites Provide accurate clinical information to all team members. 8) Adhere to clinical standards and practices in the country (ISO) and complies with SJM quality standards, legal and regulatory requirements and the SJM Code of Business Conduct. 9) Network with functional specialists in other department to ensure sharing of best practice and technical insights in a way that builds personal expertise and adds scientific and commercial value to the Company. |
| Requirements |
1) University degree in science or nursing. 2) At least 1 year of work experience as a CRA in the medical devices industry. 3) Fluent in English and French. 4) Knowledge of MS office programs. 5) Able to work independently and within a team environment. |

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