Pb Do you want to be part of a team with a real impact on global health? /b /p p At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide. /p p We are currently looking for a b Clinical Project Leader /b to join Noucor’s Clinical and Preclinical Department. /p pb Main Responsibilities /b /pp As a Clinical Project Leader, you will contribute to the planning and execution of the clinical and/or preclinical development of VAM products and/or NCEs, supporting biopharmaceutical development, clinical and preclinical studies, regulatory submissions, and post-registration activities. /p ulli Design, manage, monitor, complete, and communicate planned clinical and/or preclinical studies. /lili Ensure that clinical trials are conducted in compliance with Good Clinical Practice (GCP) guidelines and company procedures. /lili Prepare, manage, and update registration-related documentation, as well as documentation arising from deficiencies identified during clinical and/or preclinical evaluation phases. /lili Manage information and maintain communication with external clinical and preclinical experts. /lili Coordinate activities required to obtain the documentation and materials necessary for conducting clinical trials involving investigational products or new therapeutic indications for marketed products (Phase I–IV studies). /lili Perform all activities related to the design (drafting/reviewing protocols and other technical documentation), management (investigator selection, study medication, etc.), monitoring, and close-out (final report review and related procedures) of clinical trials. /lili Identify, request proposals from, and select the most suitable Contract Research Organizations (CROs) for planned preclinical studies and/or clinical trials. /lili Oversee and monitor clinical and preclinical studies outsourced to CROs and provide regular updates to the PM Manager. /lili Provide guidance and collaborate with departments and business areas involved in the preparation and/or maintenance of the product#39;s technical dossier, including Regulatory Affairs, Pharmacovigilance, and other relevant functions. /li /ul pb Requirements /b /pulli University degree in Health Sciences, preferably Pharmacy. Degrees in Human Biology, Biotechnology, or Biomedicine will also be considered. /lili Minimum of 5 years of experience in clinical studies, particularly Phase II–IV clinical trials. /lili Minimum of 2 years of experience coordinating global clinical trials as a Clinical Project Manager or Study Manager. /lili Experience in preclinical studies is considered a plus. /lili Advanced English proficiency (C1 level). /lili Strong knowledge of Good Clinical Practice (GCP) guidelines. /li /ul pb We Offer /b /pp⚙️ Work within a great team of professionals with a very good work environment. /pp❤️ Competitive benefits package and adaptable schedule. /pp️ Subsidized canteen service available on-site. /pp Free parking for employees. /ppWe care about your well-being – the Wellness Plan includes physiotherapy, online psychology services, sports events, and more. /ppOffices in Palau-solità i Plegamans. /p pb Interested in joining us? /b /pp At b Noucor /b, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic. /p p If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you. /p