Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a
The RPM will provide business support to GRA. Key member of the Project Management Team ensuring the Product strategy aligns with the Regulatory strategy and works in concert with the PMT and GRT to operationalize the
Job Title: Senior Regulatory Affairs Officer Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional & Non-Promotional Materials Review within our
Regulatory Science and Policy Associate - VIE Contract Location: United Kingdom, Reading Target start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged
Lead and execute clinical and operation advanced analytics or system improvements Develop novel data science methodologies to generate deep insights from disparate data sources. Provide subject matter expertise to teams in identification and application of the
Job Title: Pharmacovigilance Manager Location: Reading, UK Job Type: Regular, Full-Time Working Arrangements: Hybrid - 3 days per week on‑site in Reading and 2 days remote About the job As a Pharmacovigilance Manager, youll lead a
Regulatory CMC strategy manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of
As a Principal Biostatistician, you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross‑functional stakeholders in a fast‑paced, global environment. Key Responsibilities • Provide Principal‑level Biostatistics
Role Summary The Senior Human Resources Director will serve as a strategic HR leader supporting global business units within Global Clinical Development (GCD), R&D Solutions. Based in Europe, this role partners closely with senior executives on the
The CPM is responsible for execution of trial/program project management deliverables related to budgets and timelines. Evolution of CTOL and Program Coordinator. This position will primarily support the Global Program Leaders (GPLs) in management of a Clinical Team to
What if you could do the kind of work the world needs? At WSP, you can access our global scale, contribute to landmark projects and connect with the brightest minds in your field to do the
Stantec is seeking a strategic and driven Regional Commercial Lead to join our thriving UK Water business. This is a pivotal role within our South & Midlands region as our portfolio strengthens across the transformative AMP8
Regulatory Science and Policy Associate - VIE Contract + Location: United Kingdom, Reading + Target start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and
Job Title: Pharmacovigilance Manager + Location: Reading, UK + Job Type: Regular, Full-Time + Working Arrangements: Hybrid - 3 days per week on‑site in Reading and 2 days remote _About the job_ As a Pharmacovigilance Manager
Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of
Role Summary The Senior Human Resources Director will serve as a strategic HR leader supporting global business units within Global Clinical Development (GCD), R&D Solutions. Based in Europe, this role partners closely with senior executives on the
As a Principal Biostatistician , you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies , working closely with cross‑functional stakeholders in a fast‑paced, global environment. Key Responsibilities - Provide