YOUR CONTRIBUTION
As Head of Signal Evaluation & Clinical Trial Safety (m/f/d) and member of the Product Safety Leadership Team, you contribute to the development and success of the Merz Therapeutics organization. Together with your team of six, you contribute to our global clinical studies and thus actively shape the global product development of R&D from a safety perspective. Your main responsibilities will include the following activities:
- Lead and develop a team of six employees as well as taking over the planning and responsibility of the dedicated budget
- Shape clinical development programs of our neurotoxin as well as other future products from a safety perspective
- Proactively improve ongoing processes and design new global (EU and RoW) processes within your area of responsibility
- Ensure the safety of our drugs by means of "state of the art" signal management including signal detection/signal evaluation processes for marketed products and products in clinical development by owning the overall safety strategy and ongoing risk-benefit assessment
- Ensure the safety of our drugs by thorough Health Hazard Evaluations including risk assessment, categorization and profound evaluation of medical impact of manufacturing issues, quality deviations with potential product or patient risks
- Ensure the quality of regulatory documents, e.g., PSURs, EU Risk Management Plans, DSURs
- Contribute to the preparation and follow-up of audits and inspections
- Contact person for regulatory inquiries and inquiries from subsidiaries regarding drug safety
- Assess risks that may result from quality deficiencies