The Local Trial Manager role ensures top-quality end-to-end trial delivery at a country level and manages the consistency of Local Trial Management duties and processes. The manager serves as the country-level single point of contact on the study for internal partners. The Local Trial Manager manages and oversees central IRB and other local vendors and the execution of local milestones from feasibility through study close out.

The Managed Services Team comprises +90 consultants in Europe, of which +5 are in the Safety Team, and due to the rapid growth of the client portfolio, Veeva is growing the team. As a Safety Consultant, you will support a group of biopharmaceutical customers assigned to you by understanding their business processes, providing guidance, discussing Vault changes, and applying all the required configurations.

The Strategic Site Partner (SSP) serves as a key driver and main point of contact for key partner sites, strengthening strategic partnerships cross-functionally with key clinical sites in order to unlock operational potential and build strong, longitudinal relationships. The SSP is responsible for adopting relationship management principles and critically thinking to better understand all business dimensions to impact and drive operational efficiencies in the conduct of AbbVie’s pipeline.

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Proactively manage the scientific relationships between Kyowa Kirin and selected therapy area experts and academics, working collaboratively with HCPs to identify opportunities advancing clinical practice to improve patient outcomes.

This leader manages all aspects of pharmacy services, ensuring they align with Intermountain Health’s Fundamentals of Care, while fostering a culture of engaged caregivers. They support clinical and operational initiatives to achieve the best operational and clinical outcomes. This leader handles human resource responsibilities, fiscal performance, and ensures compliance with pharmacy practice regulations, and this role manages a team of less than twenty caregivers.

An UK home-based Oncology Clinical Project Manager is required to manage sites within the UK region. You will be partnering with a well-known global pharmaceutical company with a strong portfolio in multiple medicines. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

As a CRA I, II you will be joining a team supporting a long-term partnership with one of the most established pharmaceutical companies. Within this program you will find a culture focused on teamwork. You will have the opportunity to work on breakthrough technologies and this is a challenging career path that will support your growth and professional development.

As a Global Clinical Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation. The Clinical Trial Manager ensures overall successful execution of phase 1-4 clinical trials in multiple therapeutic areas, in accordance with applicable Standard Operating Procedures, agreed timelines, budgetary and regulatory requirements, at a global scale.

Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Acts as the primary quality representative for the global supply chain.