Job Summary The Associate Director of Clinical Development at Planet Pharma plays a pivotal role in shaping and executing clinical development 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.