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

JR Italy; Torino; Remoto; EUR 80.000 - 150.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a Clinical Development Director specializing in dermatology. This pivotal role involves leading clinical strategies from product development to commercialization, ensuring compliance with regulatory standards. The ideal candidate will leverage their extensive experience in clinical sciences and regulatory affairs to guide innovative dermatology products through the development lifecycle. As a key liaison among internal teams and external stakeholders, you'll foster collaboration and advocate for groundbreaking therapies. If you're passionate about dermatology and ready to make a significant impact, this opportunity is for you.

Competenze

• 10-12 years in clinical sciences and regulatory dermatology studies.
• Experience in Phase 1-3 clinical development within pharma.

Mansioni

• Evaluate clinical data to inform development strategies.
• Collaborate with various teams for planning and execution.
• Provide medical monitoring for dermatology studies.

Conoscenze

Dermatology expertise

Clinical development

Regulatory knowledge

Data evaluation

Cross-functional collaboration

Presentation skills

Formazione

MD or equivalent postgraduate medical degree

Descrizione del lavoro

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Job Reference:

636941607739850752033712

Job Views:

1

Posted:

08.05.2025

Expiry Date:

22.06.2025

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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, aligning with Glenmark’s objectives across various markets. The individual will offer strategic and tactical clinical leadership for evaluating and planning clinical development programs, preparing protocols, overseeing trial execution from a medical perspective, and managing regulatory interactions for registration trials and lifecycle management of specialty dermatology products globally. Additionally, the role involves reviewing scientific data, performing due diligence for in-licensing potential assets, and acting as a liaison among internal teams and external stakeholders throughout product development and lifecycle stages. The candidate should be a trained dermatologist 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 Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, and Intellectual Property teams 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 understanding and advocacy for products and therapeutic areas.
• Support global medical affairs by providing expertise on due diligence for licensing and acquisition of new products, including late-stage compounds and marketed products.
• Plan and oversee publication and presentation of data at international conferences, symposia, and journals, aligned with clinical data generated.
• Ensure all activities comply with Glenmark standards, SOPs, and external regulations.

Knowledge and Experience:

• MD or equivalent postgraduate medical degree in dermatology with approximately 10-12 years of experience in clinical sciences, regulatory dermatology studies, or Phase 1-3 clinical development within pharmaceutical or 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, matrix organizations, with skills in financial/resource planning and management.
• Excellent presentation and communication skills to meet scientific and commercial needs.
• Ability to coordinate with multiple stakeholders across different geographies.