Director/ Sr Director/ Executive Director- Clinical Development (Dermatology)

JR Italy; Pavia; In loco; EUR 80.000 - 120.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical industry is seeking a Clinical Sciences/Clinical Development Director specializing in Dermatology. The role involves strategic leadership in clinical development, regulatory interactions, and collaboration with various teams to drive innovative products from pre-registration to commercialization. Ideal candidates will have an MD in Dermatology and extensive experience in clinical development and regulatory processes.

Competenze

• 10-12 years of experience in clinical sciences and regulatory studies.
• Understanding of drug development processes in dermatology.

Mansioni

• Evaluate clinical data for registration strategies.
• Collaborate with various teams for protocol development.
• Provide medical monitoring of clinical studies.

Conoscenze

Communication

Leadership

Clinical Development

Regulatory Knowledge

Formazione

MD in Dermatology

Descrizione del lavoro

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Director/ Sr Director/ Executive Director- Clinical Development (Dermatology), Pavia

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EU work permit required:

Yes

Job Reference:

636941607739850752033713

Job Views:

2

Posted:

16.05.2025

Expiry Date:

30.06.2025

Job Description:

Please Note: Incumbent can be based anywhere in Europe or 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 in various markets. The person will provide strategic and tactical clinical leadership to evaluate and plan clinical development programs, prepare protocols, oversee trial execution from a medical perspective, and handle regulatory interactions for registration trials and lifecycle management of dermatology products across markets. Additionally, reviewing scientific data and performing due diligence for in-licensing potential assets will be part of the role. The individual will act as a conduit between internal and external stakeholders throughout product development and lifecycle management. Candidates should be trained dermatologists with experience in clinical sciences/clinical development for registration assets and familiarity with regulators like EU/USFDA.

Job Responsibilities:

• Critically evaluate clinical data of investigational and similar drugs to inform clinical development strategies for registration purposes.
• Collaborate with teams including Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, and Intellectual Property for planning, protocol development, execution, 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 promote scientific understanding and advocacy.
• Support global medical affairs by providing expertise on licensing and acquisition opportunities for late-stage and marketed products.
• Plan dissemination of data through publications, conferences, and journals.
• Ensure compliance with Glenmark standards, SOPs, and external regulations.

Knowledge and Experience:

• MD or equivalent in dermatology with 10-12 years of experience in clinical sciences, regulatory registration studies, or Phase 1-3 clinical development in pharma/biotech.
• Understanding of drug development processes and regulatory pathways in dermatology across markets.
• Ability to interpret complex clinical data and work in cross-functional teams within a matrix organization.
• Experience in financial/resource planning and management.
• Excellent communication and presentation skills, capable of meeting scientific and commercial needs.
• Proven ability to coordinate with stakeholders across geographies.