Search the 4 jobs at BlueRock Therapeutics

The Specialist III Bioinformatics will join BlueRock Therapeutics to develop scientific software, build and analyze bioinformatics NGS pipelines, and assist with tech transfer across teams while ensuring effective communication of computational analyses.

The Manager, Publications will execute a strategic publications plan for neurology and ophthalmology, working with authors and stakeholders to produce high-quality abstracts and manuscripts while overseeing publication processes. They will ensure compliance with legal and regulatory standards and manage external medical communications agencies.

The Research Associate II will support the development of high-quality cell lines and the cell banking process, focusing on evaluating new methods, performing cell culture procedures, and collaborating across teams. This role involves data collection and analysis, adherence to laboratory safety, and effective communication of scientific findings.

The Senior Director, Pharmacovigilance is responsible for overseeing safety monitoring of clinical trials, leading cross-functional safety management meetings, and providing subject matter expertise for regulatory submissions. This role requires close collaboration with development teams to ensure safety data is accurately reported and managed throughout the clinical development process.