Job Description: We are seeking a skilled Clinical Trials Project Manager to oversee the planning, execution, and reporting of clinical trials. In this role, you will be responsible for ensuring that trials are conducted in compliance with current GCP and other applicable requirements. Your primary goal will be to enable studies execution within planned timelines while maintaining the highest level of quality and safety standards. Key Responsibilities: Develop and manage trial plans, protocols, and budgets in collaboration with cross-functional teams. Collaborate with external vendors, such as Clinical Research Organizations (CROs), to ensure timely and cost-effective delivery of services. Conduct regular project reviews and assessments to identify areas for improvement and implement corrective actions as needed. Required Skills and Qualifications: Mandatory: Degree in Medicine, Pharmacy, or Life Science. Desired: Training/experience in Pharmacokinetics, bioequivalence studies, and relevant guidelines. Fluent in English required; communicative level in Spanish preferred. At least 3 years of experience in a similar position. Benefits: Ongoing training and professional development opportunities. A collaborative and dynamic work environment. The chance to make a meaningful contribution to the success of our organization. Others: Please note that we are an equal opportunities employer and welcome applications from all qualified candidates.