Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Programmer who shares our vision of providing clinical research excellence. Joining Pivotal as a Clinical Programmer , means that you will enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct experience with our clients and offer career growth and professional development within a scientific and data driven company. You'll have the opportunity to put your passion to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. Why Pivotal: We are passionate and fully committed with medical science while using technology, to make a positive impact We provide an exceptional experience. We take care of our employees, and we ensure everyone receives permanent mentoring and training and a push to always take one step further as well as untold international experience that will help you grow and will accompany all your life We are continuously building the company, bringing together diversity of thoughts, backgrounds, cultures, and perspectives being able to create a place where everyone feels like they belong Your responsibilities will include: Serve as the clinical database programmer for the design, validation, and implementation of clinical data management systems (e.g., EDC, eCOA, eConsent, Epro, RTSM). Collaborate on efficient database implementation for clinical studies. Identify and develop tools and process improvements to enhance team, project and business efficiencies. Provide programming support for data management activities, including database development and data validations. Collaborate with multi-disciplinary teams to meet project deadlines and budgets. Ensure compliance with SOPs, CDISC/CDASH standards, ICH, EMEA, FDA, GDPR and other regulatory requirements. Design, build, test, and update project databases, edit checks, and listings for data review. Perform post-production database updates and validations. Integrate external data in the CDMS Document work, manage tasks to meet timelines, and deliver high-quality results. Support study teams and communicate progress on assigned tasks. Attend study team meetings during study setup to ensure alignment and accuracy. Continuously develop knowledge in programming, technology, and clinical processes. Perform additional related duties as required . Required profile: Education: University degree highly recommended. Experience: At least 1 year in Data Management Systems at a CRO or pharmaceutical company. Proficiency in one or more programming languages and relational CDMS (e.g. (Medidata Rave, Zelta, Medrio, Oracle, u others). Formal accreditation in database administration and programming is highly desirable Skills: Strong problem-solving skills, attention to detail, and ability to work under pressure. Proficiency in MS Office (Word, Excel, PowerPoint). Excellent written and verbal communication skills in English. Team player with strong interpersonal and organizational skills What you can expect: Career growth resources and flexible work schedules. Training to enhance therapeutic knowledge. Exposure to dynamic work environments and new experiences Commitment to Equal Opportunity: At Pivotal, we believe that diversity and inclusion are essential to the success of our team. We are committed to providing equal employment opportunities to all candidates, regardless of race, gender, sexual orientation, disability, or any other characteristic.