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

JR Italy; Roma; In loco; EUR 90.000 - 150.000; Tempo pieno

Descrizione del lavoro

An established industry player seeks a Clinical Sciences/Clinical Development Director for dermatology, responsible for providing clinical expertise from pre-registration to commercialization. This pivotal role involves strategic leadership in clinical development programs, ensuring compliance with regulations, and collaborating with cross-functional teams. The ideal candidate will have extensive experience in dermatology and a strong background in clinical sciences, making significant contributions to product development and lifecycle management. Join a dynamic environment where your expertise will drive innovation and success in dermatological products across various markets.

Competenze

• 10-12 years of experience in clinical sciences and regulatory registration studies.
• Ability to evaluate and present complex clinical trial data.

Mansioni

• Evaluate clinical data to inform development strategies for registration.
• Collaborate with various teams for planning and execution of clinical studies.

Conoscenze

Dermatology Expertise

Clinical Development

Regulatory Interactions

Data Evaluation

Cross-functional Collaboration

Presentation Skills

Formazione

MD or equivalent postgraduate medical degree in dermatology

Descrizione del lavoro

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Job Reference:

636941607739850752033711

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 a high level of clinical expertise in Dermatology, from pre-registration to commercialization, to support Glenmark’s objectives in various markets. The person shall provide strategic and tactical clinical leadership for evaluating and planning clinical development programs, including protocol preparation, trial execution from a medical perspective, and regulatory interactions for registration trials and lifecycle management of innovative dermatology products across markets. Additionally, the role involves reviewing scientific data and performing due diligence for in-licensing potential assets. The incumbent will act as a conduit between internal teams and external stakeholders throughout product development and lifecycle management in various markets. 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.

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.
• 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.
• Provide medical and scientific expertise to global medical affairs for evaluating licensing and acquisition opportunities of new products.
• Plan and support publication and presentation of data at international conferences, symposia, and journals.
• 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 registration studies, or clinical development (Phases 1-3) in pharmaceutical or biopharmaceutical companies.
• Understanding of drug development processes and regulatory pathways for dermatology products across markets.
• Ability to evaluate, interpret, and present complex clinical trial data.
• Experience working in cross-functional teams within a complex matrix organization.
• Experience in financial and resource planning and management.
• Excellent presentation and communication skills, capable of meeting scientific and commercial needs.
• Ability to coordinate with multiple stakeholders across geographies within and outside the organization.