Provide field based scientific exchange and communication of FDA approved and pipeline products In support of FDA approved products, work within the Medical Science Liaison team's objectives Identify, establish, and maintain scientific relationships withopinion leaders regarding disease state and product specific information Facilitate scientific development of pipeline c

Strategic Leadership Provide strategic direction and leadership for the clinical development of BTC and GEA Oncology program, aligning with overall corporate goals and objectives. Clinical Development Planning Develop and execute comprehensive Global clinical development plans for Oncology in the context of BTC and GEA, including study design, protocol development, and re

The Late Development Team Lead (LDTL) is a critical role in the organization that has a significant impact on the late product lifecycle of a product or platform of products. The LDTL is accountable for leading the Late Development Team (LDT) in establishing and executing on a global product(s) strategy, which integrates scientific rationale, clinical development, nonclin

The Executive Director, Late Stage Oncology Clinical Operations will lead a team of clinical operations professionals charged with the execution and delivery of our Oncology Phase 1 3 pipeline. S/he must have extensive knowledge and experience in solid tumor clinical development from planning through approvals. This includes strategic operational planning, project cost es

The Late Development Team Lead (LDTL) is a critical role in the organization that has a significant impact on the late product lifecycle of a product or platform of products. The LDTL is accountable for leading the Late Development Team (LDT) in establishing and executing on a global product(s) strategy, which integrates scientific rationale, clinical development, nonclin

This position will provide a strategic leadership in design, oversight, analysis and reporting of pharmacometrics programs to support small and large molecule compounds in oncology from discovery through registration and post marketing. Essential Functions This position has varying responsibilities relating to clinical pharmacology, pharmacokinetics (PK), and pharmacodyna

may require a work schedule that may include working outside of "normal" work hours, to meet business demands. Occasional public contact requiring appropriate business apparel. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national

The Director, Toxicology is accountable for managing the global nonclinical regulatory and investigative toxicology of assigned Jazz portfolio products, and likewise to support his/her reports overseeing those products. They will collaborate with their direct reports and other members of the toxicology group, Early Development non clinical scientists, and members of Jazz

PsiQuantum is on a mission to build the world's first utility scale, 1 million plus qubit quantum computer, powered by breakthroughs in silicon photonics and quantum architecture. We were founded in 2015 by the world's foremost experts in photonic quantum computing and have assembled a world class team dedicated to bringing the world changing benefits of quantum computing

The Integrated Data Analytics and Statistical Programming Group (IDASP) within the Department of Data sciences is responsible for developing software for the analysis of clinical study data in accordance with departmental SOPs and guidelines. Essential Functions Attend multi disciplinary team meetings, representing the programming function. Create or review and approve pr

include leading the development of launch marketing strategies and tactics across all audiences oncologists, patients, advanced practice providers, pathologists and so on. The candidate will eventually be responsible for hiring and managing Product Managers / Senior Product Managers as launch readiness shifts into execution. The Director will work closely with a wide range

Develop and implement regulatory strategies to facilitate the progress of programs in all phases of development Serve as the Regulatory Affairs representative on project teams; assure the progress of projects by providing direction, solutions, and feedback to the teams Lead regulatory interactions with health authorities, marketing partners, and vendors for their products

Develop and lead the execution of strategic roadmap and objectives for the clinical data platform(s) Partner cross functionally to optimize Jazz's use of the clinical data platform(s) and develop/implement change management strategies to maximize adoption Provide vision, motivation, leadership, and mentoring to the Clinical Data Innovation team. Plan, hire and adapt resou

Facilitates the design, development, production and delivery of Global Clinical Development Operations (GCDO) digital systems in order to achieve operational excellence, optimize data quality and realize efficiencies wherever possible Represents their department and collaborates with Information Services (IS), Clinical Operations, Outsourcing, Medical Writing, Clinical Da

Operate, maintain, and troubleshoot catalyst test units and analytical tools used to discover new catalysts and processes that deliver value to SC businesses Specifically, evaluate catalysts in high throughput and conventional fixed bed and batch reactors using analytical hardware such as gas and liquid chromatography You will work with analytical methods such as XRD, SEM