Attiva gli avvisi di lavoro via e-mail!

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

JR Italy

Lodi

Remoto

EUR 90.000 - 150.000

Tempo pieno

Ieri
Candidati tra i primi

Aumenta le tue possibilità di ottenere un colloquio

Crea un curriculum personalizzato per un lavoro specifico per avere più probabilità di riuscita.

Descrizione del lavoro

A leading company is seeking a Director of Clinical Development for dermatology, based in Lodi or remotely. The role involves providing clinical expertise, leading development programs, and ensuring compliance with regulatory standards. Candidates should have an MD in dermatology and extensive experience in clinical development.

Competenze

  • 10-12 years of experience in clinical sciences or clinical development.
  • Understanding of drug development and regulatory pathways in dermatology.
  • Experience in cross-functional team collaboration.

Mansioni

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

Conoscenze

Clinical expertise in Dermatology
Interpreting complex clinical data
Excellent communication skills
Financial/resource planning

Formazione

MD or equivalent in dermatology

Descrizione del lavoro

Social network you want to login/join with:

Director/ Sr Director/ Executive Director - Clinical Development (Dermatology), Lodi
Job Details
  • Client: [Client Name]
  • Location: Lodi, Europe or US (remote)
  • Job Category: Other
  • EU Work Permit Required: Yes
  • Job Reference: 451015710183365017633712
  • Job Views: 2
  • Posted: 22.05.2025
  • Expiry Date: 06.07.2025
Job Description

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

The Clinical Sciences/Clinical Development Director for dermatology shall provide high-level clinical expertise in Dermatology, from pre-registration to commercialization, to support Glenmark’s objectives across markets. Responsibilities include strategic and tactical clinical leadership for evaluating and planning clinical development programs, protocol preparation, trial execution, regulatory interactions, and lifecycle management of dermatology products. The role involves reviewing scientific data, performing due diligence for licensing, and acting as a conduit between internal teams and external stakeholders. Candidates should be trained dermatologists with experience in clinical sciences/clinical development for registration assets and familiarity with regulators like EU/USFDA.

Responsibilities
  1. Critically evaluate clinical data of investigational and similar drugs to inform clinical development strategies.
  2. Collaborate with Clinical Development, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, and Intellectual Property teams for planning, protocol development, execution, and regulatory interactions.
  3. Medical monitoring and supervision of dermatology clinical studies.
  4. Develop partnerships with dermatology stakeholders, external experts, and health professionals to foster scientific understanding and advocacy.
  5. Provide medical/scientific expertise for due diligence on licensing and acquisition of new products.
  6. Plan and support publication and presentation of clinical data at conferences and in journals.
  7. Ensure compliance with Glenmark standards, SOPs, and external regulations.
Qualifications and Experience
  • MD or equivalent in dermatology with 10-12 years of experience in clinical sciences, regulatory studies, or clinical development in pharma/biopharma.
  • Understanding of drug development and regulatory pathways in dermatology across markets.
  • Ability to interpret complex clinical data and work in cross-functional teams.
  • Experience in financial/resource planning and management.
  • Excellent communication and presentation skills, capable of coordinating with stakeholders globally.
Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.