You will lead the technical evaluation phase of strategic deals, including discovery, platform demonstrations, and proof-of-concept execution. Additionally, you will act as a primary feedback conduit between customers and the product team to translate technical requirements into roadmap features.
The Data Manager is responsible for the technical development, programming, and validation of electronic Case Report Forms (eCRFs) for clinical studies. They also manage database commissioning, user administration, and ensure data quality through automated validation and maintenance of Data Management Plans.
The Project Manager will lead the end-to-end planning, execution, and monitoring of complex clinical and research projects while collaborating with cross-functional teams. They will serve as the primary point of contact for clients and partners, ensuring project delivery meets quality, regulatory, and strategic objectives.
Monitor and review clinical research data for accuracy, completeness, and consistency while ensuring compliance with study protocols and regulatory guidelines. Coordinate with interdisciplinary teams to manage data quality, support pharmacovigilance activities, and assist in the development of data assurance processes.
Lead and govern a portfolio of EU Commission and regulatory-funded projects, ensuring full compliance with grant agreements and financial regulations. Manage relationships with international consortium partners and coordinate cross-functional execution to meet scientific and commercial commitments.
