Global Regulatory Combination Products Lead

Job Introduction Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra Pharmaceuticals PLC. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here...

General Description: The Director, RIM is responsible for partnering with internal and external stakeholders in executing the RIM strategy and vision for the organization. This includes activities related to RIM resources, planning and budgeting (in partnership with IT), for key systems implementation/upgrade, monitoring and analysis of submission and...

Job Description Summary: Founded in 1998, PTC Therapeutics is a global biopharmaceutical company focused on discovery, development and commercialization of innovative treatments that bring benefits to patients suffering from rare diseases. For more than 25 years, PTC have been harnessing its scientific platforms to deliver a number of life-changing...

**About Rippling** Rippling is the first way for businesses to manage all of their HR & IT—payroll, benefits, computers, apps, and more—in one unified workforce platform. By connecting every business system to one source of truth for employee data, businesses can automate all of the manual work they normally need to do to make employee changes. Take...

**Position Summary**: We are looking for an** Associate Director, Regulatory Affairs CMC **to join our team. We are expanding our existing group of exceptionally talented and well-motivated colleagues to develop and commercialize This position will be responsible for developing and executing CMC regulatory strategies to support the expansion into...

**Role & Function** The Medicine Development Leader has the overall responsibility for bringing and representing the clinical and the medical strategy for the assigned product to the Core Asset Team (CAT), including benefit / risk evaluation, PV and Safety. **Key Responsibilities** - Provides medical and scientific expertise and perspective to inform asset...

You will also take charge if strategic direction and the oversight of global and local cross-functional CMC teams across a number of areas, in order to define and deliver contemporary CMC packages across life cycle management, market authorisation and clinical development. Your expertise in biologics and process validation will be crucial in maintaining...

We're a well-funded, venture-backed gaming startup of 18 and are looking for a highly experienced Lead PM with F2P casual or hyper-casual experience to help us build games that are unique, exciting and with lots of heart! Tasks - Lead the development & live ops of a new & exciting hybrid casual game. Define a clear product vision, strategy, and roadmap for...

Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team! **Key Responsibilities**: - Provide strategic guidance on regulatory...

**About Thermo Fisher Scientific**: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $40 billion and 100,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical...

**Description** **JOB SUMMARY**: The Regulatory Intelligence Department at Syneos Health impact decision-making at the highest levels. The team translate and refine Syneos Health regulatory intelligence from internal and external sources and combine knowledge from therapy areas and functions to deliver proactive advice outlining risks and new opportunities...

Location - Switzerland - Sectors: - Insights, Research & Data - Job type: - Full Time - Remote - Salary: - Highly Competitive Package - Contact name: - Chris Sannwald- Published: - about 2 hours ago Cranmore Executive Search is representing its a company that places a deep personal commitment to their work. They measure success by the impact they make...

We make it GmbH is a company operating nationally in Switzerland which, thanks to many years of successful experience, has a high level of expertise in the personnel services sector. Its recruitment activities are focussed on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the...

**The Opportunity**: As a member of both the Medical Affairs and ABC Leadership teams, you will assume a strategic role in the management of these Global Commercial functions by helping the functions develop, execute, and achieve their financial and operational goals by providing decision support and financial counsel while integrating and using the COE...

When you join IQVIA as an **Experienced** **CRA or SrCRA (m/w/d) **in our sponsor-dedicated department,** home-based throughout Switzerland**, you will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your...

To be successful as a global company, Sobi needs to ensure clear responsibilities at a global and regional level. This will better enable the development of a coherent and aligned strategy for all markets, as well as execution of successful launches of new products, and implementation of best practices. The role of the Global VP Marketing is to act as the...

General Description:_ Reports To: Director, Regulatory Affairs Essential Functions of the job: - Manage the preparation, assembly, review, and timely submission of Clinical Trial Application (CTA) and amendments through CTIS; Coordinate the internal response to questions from Health Authorities across Europe and provide guidance as needed. - Work cross...

**Your mission**: The Clinical Project Lead acts on behalf of the sponsor supervising all aspects of Clinical Trial activities for MoonLake’ sponsored clinical studies. The Clinical Project Lead in concert with the Clinical Development team, is accountable for achieving successful delivery of MoonLake´ clinical development activities at the project level...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Position Overview** The Associate Director, Clinical Development Science provides clinical development expertise into a multi-disciplinary team engaged in advising clients in early through late-stage development of medical products. Inpout will be provided into the design and...

**Get to Know Us** **iDeals** is a global B2B SaaS product company recognized as the most highly rated and customer-centric in a secure business collaboration market. Trusted by more than **1,000,000 users** from **175,000 companies** globally, we are on a mission to create more prosperity in the world by accelerating high-stake business decisions. We...