Jobs in Monza, Regno Unito

Please Note: Incumbent can be based anywhere in Europe or the US.

The Clinical Sciences/Clinical Development Director for dermatology shall be responsible for providing high-level clinical expertise in Dermatology, from pre-registration to commercialization of innovative products, to achieve Glenmark’s objectives across 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, and 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 role acts as a conduit between multiple internal and external stakeholders throughout the development and lifecycle of the products. The candidate should be a trained dermatologist with experience in clinical sciences/clinical development for registration assets and familiarity with regulators such as EU/USFDA.

1. Critically evaluate clinical data of investigational products and similar drugs from a clinical sciences perspective to inform clinical development strategies for registration purposes.
2. Collaborate closely with teams including Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, and Intellectual Property for planning, protocol development and finalization, execution support, and regulatory interactions.
3. Medical monitoring and supervision of clinical dermatology studies.
4. Develop and maintain collaborative partnerships with dermatology stakeholders, key external experts, and allied health professionals to promote scientific understanding and advocacy of the products and therapeutic area.
5. Provide medical/scientific expertise to the global medical affairs team on due diligence for licensing and acquisition of new products, including late-stage compounds and marketed products.
6. Plan and support the publication and presentation of data at international conferences, scientific symposia, and journals, aligned with the clinical data generated.
7. Ensure all activities comply with Glenmark standards, SOPs, and external regulations.

1. Medical degree (MD or equivalent) in dermatology with approximately 10-12 years of experience in clinical sciences, regulatory registration studies in dermatology, or clinical development (Phases 1-3) within pharmaceutical or biopharmaceutical companies.
2. Understanding of the drug development process and regulatory pathways for dermatology products across various markets.
3. Ability to evaluate, interpret, and present complex clinical trial data.
4. Experience working in cross-functional teams within a complex matrix organization.
5. Experience in financial and resource planning and management.
6. Excellent presentation and communication skills, capable of meeting scientific and commercial needs.
7. Ability to coordinate with multiple stakeholders across Glenmark's geographies.