Senior Clinical Development Medical Lead

Pfizer; Paris; Sur place; EUR 130 000 - 190 000; Plein temps

Résumé du poste

Pfizer is seeking a Clinical Development Medical Senior Manager in Paris to lead multicenter trials, ensuring scientific integrity and safety while leveraging AI-enabled approaches to trial design and data review.

The role requires MD or equivalent and extensive experience in clinical development, regulatory standards, and team leadership, with a focus on risk management and quality systems within a global biopharmaceutical setting.

Qualifications

• MD or equivalent medical qualification is required.
• Postgraduate training in medical discipline or in drug development is preferred.
• Extensive knowledge of clinical development, ICH/GCP, and adverse event management.
• Experience in leading and training large teams in clinical development.
• Demonstrated use of AI-enabled tools, automation, data visualization, or digital clinical trial technologies.

Responsabilités

• Provide input for protocol design documents and ensure high-quality protocols.
• Lead or support timely delivery of quality protocols to optimize trial efficiency and data integrity.
• Provide clinical input to data standards processes and systems (SAP, TLFs, BDR).
• Manage Informed Consent Documents per SOP and respond to external questions.
• Develop and implement the Integrated Quality Management Plan (IQMP) per SOP.
• Support oversight of independent study committees (DMCs) and endpoints adjudication.

Connaissances

Clinical trial design

Risk management

Data review

Cross-functional leadership

Communication skills

Formation

MD or equivalent medical qualification

Postgraduate training in medical discipline or drug development

Outils

AI-enabled tools

Automation

Data visualization

Description du poste

Pfizer is seeking a Clinical Development Medical Senior Manager in Paris to lead multicenter trials, ensuring scientific integrity and safety while leveraging AI-enabled approaches to trial design and data review.

The role requires MD or equivalent and extensive experience in clinical development, regulatory standards, and team leadership, with a focus on risk management and quality systems within a global biopharmaceutical setting.