Beschreibung

In this role, you will provide medical leadership and oversight for clinical projects, ensuring high-quality scientific input and guiding the Clinical Trial Team. Your day-to-day responsibilities will involve engaging with external experts, conducting safety reviews, and contributing to strategic decisions.

Anforderungen

• •Medical degree (MD)
• •At least 5 years of experience in Clinical Development within the pharmaceutical or biotech industry
• •Clinical research or clinical practice experience in CNS and in at least one therapeutic area: Cardiovascular, Immunology, or Rheumatology
• •Strong knowledge of drug development and clinical trial process
• •Direct experience interacting with Health Authorities and understanding of regulatory requirements and ICH guidelines
• •Excellent written and spoken English skills
• •Strong organizational abilities
• •Proven success in complex matrix organizations and engaging with stakeholders
• •Hands-on, results-driven mindset with urgency and accountability
• •Proactive, solution-oriented approach
• •Analytical, data-driven thinker with attention to detail
• •Shares expertise openly and contributes to collaborative learning
• •Ability to think globally and understand broader strategic context

Aufgaben

• •Provide medical leadership for assigned projects
• •Lead and oversee medical components of clinical projects
• •Ensure high-quality medical input into clinical documents
• •Contribute evidence-based insights to global clinical strategy
• •Offer medical and scientific guidance to the Clinical Trial Team
• •Deliver medical oversight during study conduct
• •Present safety review and data interpretation conclusions to leadership
• •Represent the company as a medical expert in regulatory interactions
• •Engage with external experts and committees
• •Address EC/IRB and Health Authority questions
• •Support communication and publication planning
• •Conduct literature reviews and prepare position papers
• •Provide medical training to internal teams

Benefits