Requirements: English
Company: JR Italy
Region: Monza , Lombardy
Note: Incumbent can be based anywhere in Europe or the US.The Clinical Sciences/Clinical Development Director for dermatology shall be responsible for providing a high level of clinical expertise in Dermatology, from pre-registration to commercialization of innovative products, to meet Glenmarks objectives across various markets. The person will offer strategic and tactical clinical leadership for evaluating and planning clinical development programs, including protocol preparation, trial execution from a medical perspective, and regulatory interactions for registration trials and lifecycle management of dermatology products globally. Additionally, they will review scientific data and conduct due diligence for in-licensing potential assets. The role acts as a conduit between internal teams and external stakeholders throughout the product lifecycle. The ideal candidate should be a trained dermatologist with experience in clinical sciences/clinical development for registration assets and familiarity with regulators such as the EU and USFDA.Job Responsibilities:Critically evaluate clinical data of investigational and similar drugs to inform clinical development strategies for registration.Collaborate with various teams (Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Medical Affairs, Intellectual Property) for planning, protocol development, execution support, and regulatory interactions.Provide medical monitoring and oversight for dermatology clinical studies.Develop and maintain partnerships with dermatology stakeholders, external experts, and health professionals to foster scientific understanding and advocacy.Support global medical affairs with expertise on licensing and acquisition opportunities for late-stage and marketed products.Plan dissemination of data through publications, presentations at conferences, symposia, and journals.Ensure all activities comply with Glenmark standards, SOPs, and external regulations.Knowledge and Experience:MD or equivalent postgraduate medical degree in dermatology.Approximately 10-12 years of experience in clinical sciences, regulatory registration dermatology studies, or clinical development within pharmaceutical/biopharmaceutical companies.Understanding of drug development processes and regulatory pathways for dermatology products across markets.Ability to evaluate, interpret, and present complex clinical trial data.Experience working in cross-functional teams within complex matrix organizations.Experience with financial/resource planning and management.Excellent presentation and communication skills, capable of meeting scientific and commercial needs.Ability to coordinate with multiple stakeholders across different geographies.#J-18808-Ljbffr