Medical Director RHeumatology

Barrington James; Milano; In loco; EUR 80.000 - 95.000; Tempo pieno

Descrizione del lavoro

A global CRO seeks an experienced Medical Director for their Medical Affairs team in Rheumatology. This permanent full-time role allows for impactful participation in clinical development and fosters advancement into larger pharma positions. Ideal for passionate Rheumatologists with clinical trial experience looking to transition into a new environment.

Competenze

• Medical doctor with board certification in Rheumatology.
• Experience as Principal Investigator/Sub-Investigator in Phase 1-3 clinical trials.
• Fluency in English (written and spoken).

Mansioni

• Contribute to business profile enhancement and client relationships.
• Provide medical expertise at meetings.
• Review medical data to prioritize patient safety.

Conoscenze

Project Management

Technical Understanding of Clinical Trials

Consultative Relationship Management

Medical Expertise

Formazione

Medical Doctor (MD, MBBS, MB ChB, dr. med)

Board-certification in Rheumatology

Descrizione del lavoro

I am partnered with a global CRO (Contract Research Organisation) who are looking for a permanent Medical Director to lead their Medical Affairs department within Rheumatology.

This is a fantastic opportunity for an experienced clinical specialist to take on their first role in pharmaceutical industry, whilst also maintaining seniority and participating in clinical development with multiple sponsors. Successful directors go on into large pharma to become Clinical Program Leaders, Medical Directors, Executives and more!

If you are a passionate Rheumatologist wanting to branch out your clinical trial experience into a new environment, then please read below

• Responsibilities
• Be a key contributor in raising the business profile to ensure the client are the preferred partner for their clients with support on their projects
• Share your vast medical expertise at investigator meetings, kick-off meetings, and client face-to-face meetings
• Maintain a strong consultative relationship with the client throughout the project lifecycle
• Provide input into the creation of the protocol and other study-related documents
• Participate in discussions with regulators, key opinion leaders, senior management and our clients
• Deliver training to external project teams and colleagues
• Review medical data on the indication, inclusion / exclusion criteria and other medical issues to ensure overall project deliverables are achieved and patient safety prioritised
• Collaborate with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plans
• Requirements
• Medical doctor (MD, MBBS, MB ChB, dr. med)
• Board-certification in Rheumatology
• Experience as a Principal Investigator / Sub-Investigator in Phase 1-3 clinical trials
• Strong project management experience and a high level of technical understanding regarding clinical trials
• Fluency in English (written and spoken)
• Ability to work on-site in Milan, Madrid, Berlin, Mannheim, Reading or Sofia
• Job Types
• Full-time, Permanent
• 80,000.00 - €95,000.00 per year