lavori presso MD in località Singapore

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 a high level of 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 for the evaluation and planning of clinical development programs, protocol development, trial execution from a medical perspective, regulatory interactions for registration trials, and lifecycle management of dermatology products. Additionally, the person shall review scientific data and perform due diligence for in-licensing potential assets. They will act as a conduit between internal teams and external stakeholders throughout the product lifecycle 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:

• Critically evaluate clinical data of investigational products and similar drugs to inform clinical development strategies for registration purposes.
• Collaborate with teams such as Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, and Intellectual Property for planning, protocol development, execution support, and regulatory interactions.
• Provide medical monitoring and supervision of 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 and oversee publication and presentation of data at conferences, symposia, and journals.
• 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 registration studies, or clinical development in pharma/biopharma.
• Understanding of drug development processes and regulatory pathways for dermatology products in various markets.
• Ability to interpret complex clinical data and work effectively in cross-functional, matrix organizations.
• Experience in financial/resource planning and management.
• Excellent communication and presentation skills, capable of coordinating with multiple stakeholders across geographies.