Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team, managing clinical trials across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. You will lead CRAs and oversee all clinical aspects of your study. We address the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world.

Veeva Systems is looking for Consultants and Senior Consultants who have some content management expertise and/or, clinical trials expertise and/or software implementation expertise. As a member of the Professional Services team, you will be responsible for understanding our customers’ challenges and clinical needs, translating requirements into solution design, delivering training, and supporting customers during application validation.

This position delivers industry-leading services, which include call center staffing for responding to product information requests, identifying and in-taking of adverse events and/or product quality issues, and medical writing which are all fundamental to building credibility and strengthening relationships with healthcare providers, patients, and industry clients.

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.

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader. Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process. Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management. Contributes to achieving company´s goals and objectives.

Experience Biopharma Regional CRA/clinical research associate (ideally residing in Northern England/Scotland) required for Global Pharmaceutical company. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement.