Clinical Development Medical Director (Neuroscience)

Novartis; London; On-site; GBP 90,000 - 150,000; Full time

Job summary

An established industry player seeks a Clinical Development Medical Director to lead global clinical programs in neuroscience. This role involves providing strategic medical input, overseeing clinical trials, and collaborating with cross-functional teams to drive innovation in drug development. The ideal candidate will have a strong background in clinical research, particularly in neurology or related fields. Join a passionate community dedicated to reimagining medicine and making a significant impact on patient lives. This is a unique opportunity to shape the future of healthcare through innovative solutions.

Qualifications

• MD or equivalent medical degree with specialized training.
• 4+ years of clinical practice experience in neurology or related fields.

Responsibilities

• Provide clinical leadership for clinical deliverables and protocols.
• Lead development of regulatory documents and oversee clinical trials.

Skills

Clinical Leadership

Data Interpretation

Regulatory Knowledge

Team Management

Strategic Medical Input

Education

MD or equivalent medical degree

Specialized training and certification

Job description

Clinical Development Medical Director (Neuroscience)

Join to apply for the Clinical Development Medical Director (Neuroscience) role at Novartis.

Overview

The Clinical Development Medical Director (CDMD) is the global clinical leader responsible for defined program activities and deliverables (e.g., submission activities, briefing books), or clinical trials, under the leadership of the GPCH or Sr CDMD.

Key Responsibilities

• Provide clinical leadership and strategic medical input for all clinical deliverables within assigned programs, including protocols, data review, standards, regulatory documents, and publications.
• Lead development of clinical sections of regulatory documents such as Investigator’s Brochures, briefing books, safety updates, and submission dossiers.
• Drive execution of clinical programs in collaboration with global functions, Clinical Trial Heads, and regional medical teams.
• Offer medical oversight of trials, act as medical monitor, and contribute to data analysis, interpretation, and reporting (CSRs, publications, presentations).
• Support safety assessments, monitor safety data, and participate in safety management teams and safety reporting.
• Contribute to the development of disease-specific standards and provide medical input into project reviews.
• Represent Novartis in interactions with external stakeholders, including regulatory authorities, key opinion leaders, and advisory boards.
• Collaborate with research and business development teams on project transitions and target identification.
• Mentor and develop clinical team members, supporting onboarding, training, and career growth.

Minimum Requirements

• MD or equivalent medical degree.
• Specialized training and certification in a medical/scientific area, with preferred Board certification.
• At least 4 years of clinical practice experience, preferably in neurology, cell/gene therapy, rare or neuromuscular diseases, or neuroinflammation.

Work Experience

• Minimum of 5 years in clinical research or drug development, with experience in phases I-IV trials, especially in late-phase development.
• Strong scientific acumen, data interpretation skills, and knowledge of therapeutic area.
• Experience in managing teams, ideally in a global or matrix environment.

Why Join Novartis?

Our purpose is to reimagine medicine to improve and extend lives. Join us to be part of a passionate community dedicated to innovation and patient impact. Learn more: https://www.novartis.com/about/strategy/people-and-culture