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
A data collection company in Basel is seeking native speakers for a conversational audio data collection project. Participants will engage in natural conversations on suggested topics, contributing to the development of speech recognition and conversational AI
Company description Terry Soot Management Group (TSMG) is a field data collection company founded in 2017 in Europe. We collect data where automation is not possible. We count features, take pictures, make videos, record speech, and
IT – Graduate Programme IT Department Baar, Switzerland We are one of the world’s largest globally diversified natural resource companies. We mine, refine, market and cycle a wide range of raw materials that have become an
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
Responsible for providing medical and scientific support across clinical development activities, with emphasis on protocol development and study design review, clinical data interpretation, site and PI interaction, regulatory response documents, ongoing safety review, and medically relevant
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
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our