Responsibilities: You will be responsible for scientific input to clinical development strategies and therapeutic areas. Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full
Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during
Job Description Location: While a primarylocation is identified for this role, qualified internal candidates located in Cambridge, MA, USA may also be considered, subject to business needs, role requirements, talent availability, and local legal requirements. Compensation:
Takeda in Switzerland is seeking a senior leader to drive Global Patient Access (GPA) strategy and operations. You will influence cross-functional stakeholders to deliver integrated patient-centric strategies aligned with regulatory and product lifecycle needs.You will leverage data, analytics,
Director, Vaccines Medical Program Management About the role Provide strategic program leadership for the most critical and complex Medical priorities, ensuring that enterprise Medical strategies are translated into executable portfolio plans, governed effectively, and delivered with
Responsibilities:• Manages and directs functions to comply with standard operating procedures, regulatory safety and pharmacovigilance and business technology quality standards in compliance with national and international regulations, such as relevant GxP guidelines and national and international
Position Summary The Senior Director, Head of Medical Evidence reports into the Vice President, Head of Disease Areas and coordinates with Medical Affairs and cross-functional stakeholders to lead the Integrated Evidence Generation Plans (IEGP) for all
Explore a new world of possibilities As a key part of the HomeToGo Group, Interhome is united by a vision to be the world’s number one for holiday home rentals. We combine decades of industry expertise
The Director Non-Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology
The Director of Intellectual Property provides strategic support to CSL Research and Technical Operations organizations, with a primary responsibility for Tech Ops activities in Bern and Research in Schlieren (Zurich). In particular, the role will support
Make an impact with NTT DATA Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and
Make an impact with NTT DATA Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and
At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities, collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our