Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Join Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist (location: Switzerland, Home-based), you will play a pivotal role in
About Lucid At Lucid, we are creating exceptional mobility experiences through innovation to drive the world forward. Built on Lucid’s proprietary technology and software-defined vehicle architecture, our award-winning vehicles bring our “Compromise Nothing” approach to the
Start date: Between October and November 2026 (subject to agreement) We are looking for a European lawyer to join our legal team on a maternity cover basis. This is an in-house role for a lawyer who
Start date: Between August and October 2026 (subject to agreement) We are seeking a Compliance Analyst for the KYC team within our Corporate Compliance team in Baar, Switzerland, on a temporary basis (12 months). In this
Job Title: Regional Study Start-Up Lead About This Role: As a Regional Study Start-Up Lead, you will play a pivotal role in managing the effective delivery of site activation within your designated region(s). For this particular
Description For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore
Join us in shaping the future of user engagement and personalization at MDPI. As a Product Owner, you will work closely with stakeholders and development teams to deliver innovative, data-driven product experiences across our digital platforms.
Department: Iron Ore Marketing Internship duration: 6 months Start date: as soon as possible For motivated candidates, we offer the chance to join one of the world’s largest producers and marketers of commodities, and to become
Business IntroductionAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining
Start date Between October and November 2026 (subject to agreement) Responsibilities Oversee legal aspects of HSEC and human rights programmes, including regulatory compliance and risk management. Provide legal support to the Responsible Sourcing team in connection
At Novocure, every role contributes to extending the lives of people living with cancer. As our new Senior Director, Clinical Regulatory Affairs, you’ll play a key part in this mission. This is a highly visible global
Start date:Between October and November 2026 (subject to agreement)We are looking for a European lawyer to join our legal team on a maternity cover basis. This is an in‑house role for a lawyer who has a
Associate Safety Director (m/f/d) (LSW)- Drug safety/pharmacovigilance/ English Background: Portfolio Safety Scientists (PCS-Sci) provide safety science and pharmacovigilance support to molecules across the Roche portfolio. As a group, they are responsible for all aspects of safety
Who We Are: Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines,
GSK is seeking a Clinical Sciences Leader in Global Clinical Oncology R&D to deliver high-quality study strategy and design across global oncology studies. You will lead end-to-end protocol development, contribute to informed consent forms, and oversee data interpretation
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