.Make your mark for patients.
We're here because we want to build the future and transform patients' lives for the better.
At UCB, our people are our experiences and achievements, our passion and drive.
That's why we're looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients.
We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead.
Will you join us in pushing the boundaries of what's possible?Hiring Manager: Barbara Schruff, Clinical Research Associate Team LeadTo strengthen our Development Solutions department, based in Madrid, Spain we are looking for a talented individual to fill the position of Senior Clinical Research Associate.As a Senior Clinical Research Associate you will maximize site performance and site engagement in UCB conducted clinical studies, leveraging strong clinical operational and therapeutic expertise to support execution of the clinical studies.You like to work in an environment where you can:Be part of a diverse and great collaborative team.Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of UCB and its activities thereby increasing their desire to partner with UCB.Be part of an ambitious organization with promising biopharma products pipeline and development opportunities.You will contribute by:Being responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with UCB Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements.Engaging with clinical sites to develop, build, and maintain strong relationships with investigators/staff that will ensure high quality investigative sites to support UCB's clinical development programs.Collaborating with internal and external stakeholders as well as third party vendors.Providing operational support to the CPM/Sr CPM to deliver the study within planned timelines and according to required standards of quality and compliance.Evaluating, screening and developing high quality investigative sites to support UCB's clinical development programs.Interested?
For this position you'll need the following education, experience and skills:A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e.G.
clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies).S., M.S.
degree in a life science/biological related field preferred