Top Tech Jobs & Startup Jobs

The Study Startup Specialist coordinates initiation of clinical trials, manages regulatory submissions, oversees site activation, and ensures compliance with guidelines.

The Director of Biostatistics leads statistical support for clinical development projects, collaborates on regulatory submissions, mentors staff, and ensures compliance with regulatory requirements.

The Manager of GCP/GVP Quality and Compliance ensures adherence to GCP/GVP regulations, conducts audits, and supports compliance training across teams.

Support the Director of CTDO in executing strategies, enhancing department efficiency, coordinating with various departments, and managing investor relations and global conference logistics.

Collaborate on clinical studies, providing statistical support and data analysis using SAS and R, and oversee CRO programming activities.

Lead and advance protein engineering projects using cutting-edge techniques, conduct data analysis, and supervise junior scientists while ensuring lab safety and compliance.

The role involves leading upstream process development for biopharmaceuticals, including bioreactor operations, process optimization, and technology transfer for CHO cells in clinical manufacturing.

Manage pharmacovigilance operations, vendor oversight, compliance, training, and quality management, ensuring adherence to regulations and safety data processing.

The IT Infrastructure Specialist will manage server administration, network security, storage, and provide end-user support while collaborating with IT teams on projects.

Lead SystImmune's business development efforts, including strategy execution, partnership development, team leadership, and external communications to drive growth and clinical asset progress.