Jobs in Torino, Italie

Please Note: Incumbent can be based anywhere in Europe or 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 achieve Glenmark’s objectives in various markets. The person shall provide strategic and tactical clinical leadership to enable successful evaluation and planning of clinical development programs, protocol preparation, trial execution from a medical perspective, regulatory interactions for registration clinical trials, and lifecycle management of innovative, specialty dermatology products across various markets. Additionally, the person shall review scientific data and perform due diligence for in-licensing potential assets. The individual shall act as a conduit between multiple internal and external stakeholders throughout the development and lifecycle of the products in various markets. The candidate should be a trained dermatologist with experience in clinical sciences/clinical development for registration assets and familiarity with regulators including EU/USFDA.

Job Responsibilities:

1. Critical evaluation of clinical data of investigational products and similar drugs to build a foundation for clinical development strategies for registration purposes.
2. Collaborate with various teams (Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, Intellectual Property) for planning, protocol development and finalization, execution support, regulatory interactions, etc.
3. Medical monitoring and supervision of dermatology clinical studies.
4. Develop and maintain partnerships with dermatology stakeholders, external experts, and allied health professionals to ensure scientific understanding and advocacy.
5. Provide medical/scientific expertise to global medical affairs for due diligence on licensing and acquisition of new products.
6. Plan publication and presentation of data at international conferences, symposia, and journals.
7. Ensure all activities comply with Glenmark standards, SOPs, and external regulations.

Knowledge and Experience:

• Medical degree (MD or equivalent) in dermatology with 10-12 years of experience in clinical sciences, regulatory studies, or Phase 1-3 clinical development in pharmaceutical/biopharmaceutical companies.
• Understanding of drug development processes and regulatory pathways for dermatology products in various markets.
• Ability to evaluate, interpret, and present complex clinical trial data.
• Experience working in cross-functional teams within a complex matrix organization.
• Financial and resource planning experience.
• Excellent presentation and communication skills, capable of meeting scientific and commercial needs.
• Ability to coordinate with stakeholders across Glenmark's geographies and external partners.