Clinical Development Director - CRM **80-100%

Summary

-Oversees the planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations. Establishes and approves scientific methods for design and implementation of clinical protocols, data collection systems and final reports. Support new and ongoing clinical research and clinical trials and ensure efficient and timely processing of confidentiality agreements and clinical agreements

About the Role

Are you ready to take the next step in your career as a Clinical Development Director? We have an exceptional opportunity for a highly motivated individual to join our team at Novartis, a world-class pharmaceutical company located in Switzerland.

At Novartis, we are committed to pushing the boundaries of medical research and development. As the Clinical Development Director, you will play a crucial role in our research efforts, helping us to bring life-changing treatments to patients around the globe. This is not just another research role; it is a chance to make a real difference and contribute to groundbreaking advancements in medicine.

• Lead and oversee the clinical development strategy for our CRM (Clinical Research Management) program.
• Collaborate with cross-functional teams to design and implement clinical trials, ensuring flawless execution and adherence to timelines.
• Drive the development and execution of clinical protocols, monitoring the progress of studies and making necessary adjustments to ensure successful outcomes.
• Analyze and interpret clinical trial data, providing insights and recommendations to support decision-making processes.
• Stay up-to-date with the latest scientific advancements and regulatory requirements, ensuring compliance at all times.
• Foster a culture of innovation and collaboration, mentoring and developing team members to reach their full potential.
• Build strong connections with external individuals and groups, such as influential figures and regulatory bodies.

• Advanced degree in life sciences / healthcare (or clinically relevant degree) is required. PharmD or PhD is strongly preferred
  • Minimum 7 years experience in clinical research or drug development
  • Working knowledge of the assigned disease area (Cardiovascular) is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level
• In-depth knowledge of clinical trial design, execution, and regulatory requirements.
• Strong analytical and problem-solving skills, with the ability to determine appropriate actions based on data analysis.
• Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.
• Strong collaboration skills and the ability to work effectively with diverse teams from different departments.
• A passion for making a difference in the lives of patients and a commitment to upholding the highest ethical standards.