Clinical Trial Associate
The Clinical Trial Associate manages the Study Master File and coordinates practical study tasks. The role offers professional growth within a global CRO environment.
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89,000+ live jobsThe Clinical Trial Associate manages the Study Master File and coordinates practical study tasks. The role offers professional growth within a global CRO environment.
Senior Project Managers will lead clinical trials in dermatology and rheumatology. The role involves managing project lifecycles, budgets, and client relationships.
You will manage digital campaigns, social media, and content creation to support business growth. The role offers exposure to European marketing activities in a scientific services organization.
This role leads product safety for complex clinical studies, managing data collection and regulatory reporting. You will oversee safety management plans and collaborate with global stakeholders.
This role involves leading the development of medical writing strategies and clinical pharmacology documents. It offers a collaborative environment with competitive benefits and career development.
This role involves patient care and laboratory sample management. You will handle sample labeling, stock control, and administrative tasks. The position is based on-site in Sant Cugat del Vallès.
This role manages service contract administration, including order processing, tender support, and customer quotes. It offers the chance to work in a global life sciences company.
Caregivers will maintain experimental animals and perform cleaning and sanitation of facilities and equipment. The role offers paid training and a 40-hour weekly schedule.
Provide administrative and organizational support to the CEO and Managing Directors. You will coordinate events, manage calendars, and handle travel arrangements.
This role involves drafting, reviewing, and negotiating supplier contracts while managing the full contract lifecycle.
This role leads the end-to-end execution and delivery of global clinical studies. You will manage cross-functional teams, stakeholders, and vendor relationships. The position is based in Reading, UK.
This role involves monitoring clinical sites to ensure regulatory and protocol compliance. It offers career development and technical training within a global life sciences organization.