Role OverviewThe Associate Director of Clinical Development plays a pivotal role in shaping and executing clinical trial strategies. This position involves close collaboration with cross-functional teams to advance therapeutic programs from concept through execution. The ideal candidate will possess a strong foundation in clinical research and drug development, with the ability to translate scientific insights into actionable clinical plans.
Key ResponsibilitiesDesign and implement clinical development programs aligned with regulatory and strategic goalsSupport the creation of protocols, study reports, investigator brochures, and other clinical documentationCollaborate with teams across biostatistics, regulatory affairs, medical affairs, and clinical operations to ensure high-quality trial deliveryAnalyze and interpret clinical data to guide decision-making and support regulatory submissionsStay informed on scientific and competitive developments within relevant therapeutic areasProvide scientific input during interactions with investigators, regulatory bodies, and key opinion leadersContribute to the preparation of regulatory submissions including INDs, NDAs, and clinical sections of filings
QualificationsBachelor’s degree in Life Sciences, Pharmacy, or a related field;
MD or equivalent advanced degree preferredMinimum of 1–2 years of experience in clinical research or development, ideally within pharma, biotech, or CRO environmentsTechnical SkillsFluent in English;
additional languages are a plusProficiency with productivity and collaboration tools (e.G., Google Workspace, MS Office)Familiarity with medical terminology and clinical trial design principlesAdditional RequirementsStrong grasp of clinical trial methodologies, regulatory standards, and statistical conceptsExperience in scientific writing and preparation of clinical and regulatory documentsAbility to interpret complex clinical data and communicate findings effectivelyExcellent interpersonal and collaboration skills within cross-functional teams