Responsibilities: Responsible for supporting the clinical development Neuroscience team with medical and safety monitoring. Provides medical monitoring and observation of clinical trials to ensure safety and adherence to protocol. Coord...
Responsibilities: Support the Lead Data Manager across one or more clinical studies. Reviews protocols for appropriate data capture including electronic (eCRF) design. Support CRF design, review, and validation of clinical database. Pr...
Responsibilities: Responsible for supporting the clinical development Neuroscience team with medical and safety monitoring. Provides medical monitoring and observation of clinical trials to ensure safety and adherence to protocol. Coord...
Responsibilities: However, they will mainly fall within the areas of Pharmaceutical, Biotechnology or Biologics Regulatory Affairs. This individual will prepare, compile, and submit CT/IND/MAA I NOA, manage and implement label review, tr...
Job Description: Seeking a Contract Scientist to support the siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This temporary position offers the opportunity to contribute to the design and execution of cutting-...
Responsibilities: Lead and mentor high-performance teams of Test Analysts/ Engineers, in geographically distributed locations, effectively to deliver testing-related project deliverables on time, on budget, and with high quality. Effecti...
Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validat...
Responsibilities: Lead the design of data collection and management systems and initiate process improvements as needed. Establish goals, timelines, and deliverables for data management of trials, and oversee priorities and timelines for...