PbDo you want to be part of a team with a real impact on general health? /b /ppbr/ppAt Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide. /ppbr/ppWe are currently looking for a bClinical Project Leader /b to join Noucor’s Clinical and Preclinical Department. /ppbr/ppbMain Responsibilities /b /ppAs 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. /ppbr/pulliDesign, manage, monitor, complete, and communicate planned clinical and/or preclinical studies. /liliEnsure that clinical trials are conducted in compliance with Good Clinical Practice (GCP) guidelines and company procedures. /liliPrepare, manage, and update registration-related documentation, as well as documentation arising from deficiencies identified during clinical and/or preclinical evaluation phases. /liliManage information and maintain communication with external clinical and preclinical experts. /liliCoordinate 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). /liliPerform 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. /liliIdentify, request proposals from, and select the most suitable Contract Research Organizations (CROs) for planned preclinical studies and/or clinical trials. /liliOversee and monitor clinical and preclinical studies outsourced to CROs and provide regular updates to the PM Manager. /liliProvide guidance and collaborate with departments and business areas involved in the preparation and/or maintenance of the product's technical dossier, including Regulatory Affairs, Pharmacovigilance, and other relevant functions. /li /ulpbr/ppbRequirements /b /pulliUniversity degree in Health Sciences, preferably Pharmacy. Degrees in Human Biology, Biotechnology, or Biomedicine will also be considered. /liliMinimum of 5 years of experience in clinical studies, particularly Phase II–IV clinical trials. /liliMinimum of 2 years of experience coordinating global clinical trials as a Clinical Project Manager or Study Manager. /liliExperience in preclinical studies is considered a plus. /liliAdvanced English proficiency (C1 level). /liliStrong knowledge of Good Clinical Practice (GCP) guidelines. /li /ulpbr/ppbWe Offer /b /pp⚙️ Work within a great team of professionals with a very good work environment. /pp❤️ Competitive benefits package and flexible schedule. /pp ️ Subsidized canteen service available on-site. /p