Job Opportunities API

You will provide oversight of biostatistical activities across clinical trials and real-world evidence studies, including the management of CROs supporting MA and BLA submissions. You contribute to statistical analysis planning, and contibute to the development of high-quality regulatory deliverables including ISS, ISE, SCS and SCE. Provide oversight and direction to CROs and external vendors deliverig statistical services for clinical trials and RWE data, ensuring quality, compliance and timely delivery witin budget.You provide input into the development of integrated safety and efficacy documents (ISS, ISE, SCS and SCE) in collaboration with regulatory and medical writing teams. You do have experience on the sponsorside, preferably also on the CRO side.You need to have >10 years of relevant experience. Please indicate your availability (as of when and how many hours a week) and your hourly/daily rate