Position Summary The Associate Director – Clinical Development plays a pivotal role in shaping and executing clinical development strategies. This individual will be responsible for the design, implementation, and interpretation of clinical trials, working collaboratively with cross-functional teams to advance the development pipeline. The ideal candidate brings a strong foundation in clinical research and drug development, with the ability to translate scientific insights into actionable clinical strategies. Key Responsibilities Design and oversee clinical development programs aligned with regulatory and business goals. Contribute to the development of clinical protocols, study reports, investigator brochures, and other essential clinical documents. Collaborate with cross-functional teams including biostatistics, regulatory affairs, medical affairs, and clinical operations to ensure seamless trial execution. Analyze and interpret clinical trial data to support decision-making and regulatory submissions. Monitor scientific and competitive developments in relevant therapeutic areas to inform clinical strategy. Provide scientific input for interactions with investigators, regulatory authorities, and key opinion leaders. Support the preparation of regulatory submissions including INDs, NDAs, and clinical sections of global filings. Qualifications Education: Bachelor’s degree in Life Sciences, Pharmacy, or a related field. Advanced degree (MD or equivalent) Experience: Minimum of 1–2 years in clinical research or clinical development within the pharmaceutical, biotechnology, or CRO industry. Technical Skills & Competencies Fluent in English; proficiency in Italian is a plus. Proficient with productivity and collaboration tools (e.g., Google Workspace, Microsoft Office). Solid understanding of medical terminology and clinical trial methodologies. Familiarity with regulatory frameworks and statistical principles in clinical research. Strong scientific writing skills, including experience drafting clinical protocols and regulatory documents. Ability to interpret complex clinical data and communicate findings effectively to diverse stakeholders. Excellent interpersonal and collaboration skills in a cross-functional environment. #J-18808-Ljbffr