Manager, Clinical Trial Transparency

Responsible to plan, lead and coordinate activities for submissions documents related to redaction/anonymization activities for Health Canada PRCI and EMA Policy 0070. Ability to work independently with project team, develop a schedule designed to meet necessary deadlines for a particular project, communicate with team members about that schedule, and track the progress to assure the timely completion of the tasks. The person is accountable to set up a process for the respective task, identify any risks, consider the cross-functional collaboration and feedback on an ongoing basis.
**What you will be doing**:
- Leads and establishes the process for- either the redaction/anonymization activities of personal data/company confidential information in clinical documents according to applicable guidelines and local laws as well as ensures timely delivery of anonymization reports when applicable and / or
- Participates to the development and maintenance of- the commercial confidential...