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TFS HealthScience is a global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to bring new treatments to market.
As an EU Director of Regulatory Affairs, you will lead global regulatory strategies for drugs and devices. The role involves supporting business development and managing EMA scientific advice.
Senior Medical Director for oncology/hematology at a global CRO, acting as medical monitor and portfolio medical lead.
The Drug Safety Associate handles drug safety and vigilance issues according to regulatory requirements. You will support SAE handling, case reviews, and safety database entries.
A Senior Project Manager will lead multidisciplinary oncology study teams to ensure clinical milestones are met. The role offers competitive compensation and professional growth opportunities.
This role offers hands-on experience in HR operations within a global organization. You will support the full employee lifecycle, including onboarding, administration, and HR projects.
This role leads the development and scaling of clinical database programming capabilities. You will drive change leadership, manage technical escalations, and improve governance models.
Clinical Research Manager to oversee clinical trial operations within the Ophthalmology team. The role involves managing site activities, leading CRAs, and ensuring regulatory compliance.
Senior Project Manager to lead cross-functional clinical projects and ensure delivery. The role involves managing timelines, budgets, and multidisciplinary teams.
A Senior Quality Manager will provide functional and project-level quality oversight within a clinical research organization.
The Veeva Vault Administrator manages and configures the Veeva Vault platform to support clinical and regulatory processes.
TFS HealthScience is a global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to bring new treatments to market. With over 30 years of experience, the company provides a comprehensive range of clinical development services, including project management, clinical monitoring, data management, biostatistics, regulatory affairs, and quality assurance. TFS operates across North America, Europe, and Asia, employing a team of clinical and scientific professionals dedicated to advancing healthcare through efficient and compliant clinical trials.
In Spain, TFS HealthScience has established a strong presence with offices in Madrid and Barcelona, serving as a key hub for clinical operations in Southern Europe. The company is known for its collaborative and supportive work culture, offering international professionals the opportunity to work on diverse therapeutic areas and global studies. For those relocating to Spain, TFS provides a dynamic environment that values professional growth, cross-cultural collaboration, and work-life balance, making it an attractive employer for clinical research and quality management experts.
TFS HealthScience was founded in 1991 and has grown into a global contract research organization (CRO) providing clinical development services to the pharmaceutical, biotechnology, and medical device industries. The company has expanded its footprint across North America, Europe, and Asia, offering a full range of clinical trial services from feasibility and regulatory affairs to data management and biostatistics.