Clinical Development Director in Dermatology (Clinical Program Leader)-M/F

TN France; Toulouse; Hybride; EUR 80 000 - 120 000; Plein temps

Résumé du poste

An established industry player is seeking a Clinical Program Leader in Dermatology to drive innovative clinical studies. In this pivotal role, you will collaborate with cross-functional teams to ensure the highest standards of patient safety and scientific integrity. Your expertise will guide the development of clinical documents and the execution of clinical trials, making a significant impact on the advancement of dermatological therapies. If you are a self-motivated leader with a passion for clinical development, this opportunity offers a chance to shape the future of patient care in a dynamic environment.

Qualifications

• Ph.D. or Physician with 5+ years in clinical development in biotech/pharma.
• Experience in leading clinical studies and managing cross-functional teams.

Responsabilités

• Develop and manage clinical studies in Dermatology diseases.
• Ensure patient safety and compliance with regulatory guidelines.
• Act as medical expert and represent the company in public sessions.

Connaissances

Leadership

Communication

Problem Solving

Organizational Skills

Collaboration

Negotiation

Formation

Ph.D. in Immunology

Physician specialized in Dermatology

Description du poste

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Clinical Development Director in Dermatology (Clinical Program Leader)-M/F, Toulouse

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Client:

Location:

Toulouse, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

55fe635e6416

Job Views:

1

Posted:

29.04.2025

Expiry Date:

13.06.2025

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Job Description:

Your mission

We are seeking a talented and highly motivated Clinical Program Leader in Dermatology (Clinical Development Director) to develop and enhance experience in design and management of clinical studies in Dermatology diseases, working in collaboration with the Clinical Team.

You will support the relevant clinical studies for the medical/scientific aspects, especially those requiring this therapy area expertise, where you are deeply committed to acting as the main reference point.

You will contribute to the production of the Common Technical Document, in terms of validation of scientific documents relevant to the concerned clinical studies (e.g., study protocol, CRF, Investigator Brochure, clinical study report), also representing the Company in front of the institutional authorities concerned.

• Work in close collaboration with the BD department to scout and assess multiple assets to grow the pipeline in Dermatology.
• Act as Medical Expert, in cooperation with other Study Team Members, to deliver results of the assigned Clinical Studies and related Key Clinical Documents, in accordance with the Clinical Development Plan and the related agreed timelines.
• Responsible for interpretation of clinical data.
• Ensure the safeguard of Patients Safety: in collaboration with and in support of Corporate Pharmacovigilance. Ensure the ongoing risk-benefit assessment, caring for the safety and efficacy signal detection/response during conduct of assigned studies.
• Aim at meeting the needs of internal and external stakeholders, acting as Subject Matter Expert in the assigned product(s) and relevant disease(s) area, maintaining and enhancing knowledge, securing timely publication of all clinical data.
• Ensure application of up-to-date trial designs by partnering with all relevant disciplines.
• Cooperate in the design of post-registration clinical studies.
• Organize EU and extra-EU Advisory Boards. Represent the Company in front of Institutional Authorities, representing Pierre-Fabre Clinical Expertise in public sessions of Data Safety Monitoring Board Meetings.
• Act as medical writer/reviewer when required and in general act in compliance with ICH/GCP, SOPs, and Regulatory Guidelines.
• Accountable for the delivery of high-quality scientific and clinical assessment of new product opportunities for in-licensing in Dermatology, including the hypothesis for the clinical development plan (including standardized costs) and life-cycle management, and the clinical/development risks.

High flexibility about the location of this position.

Who you are?

Ph.D or Physician specialized in immunology and/or Dermatology with at least 5 years of experience in clinical development in biotech/Pharma industry.

Skills

Goal-oriented, excellent communicator, work collaboratively.

Defines operational priorities and assigns ambitious and demanding objectives.

Able to lead, negotiate and solve problems, influence the quality of the deliverables.

Excellent organizational skills, with ability to multi-task and prioritize work.

Excellent English written and oral, presentation and communication skills.

Great leadership skills and experience working in dynamic multidisciplinary environment.

Self-motivated and collaborative with ability to work with multi-disciplinary teams and external partners.