Role Summary
The Clinical Research Director, Immunology & Inflammation (Rheumatology) leads the creation and execution of the clinical development plan for one or more assets, advancing scientific and clinical knowledge in immunology and rheumatologic diseases. The role focuses on developing innovative therapies for autoimmune and inflammatory diseases, with emphasis on rheumatology, and requires collaboration across cross-functional teams and external stakeholders. Location: Cambridge, MA / Morristown, NJ.
Responsibilities
- Create clinical development strategy and plans for one or more assets
- Lead and coordinate cross-functional teams to design, implement, and execute clinical development plans and studies
- Align clinical development strategy with the global project team and internal partners, such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing
- Advance the clinical development plan through internal management review
- Lead a clinical sub team to design clinical studies and to create study protocols
- Execute the clinical development plan in close collaboration with clinical operations
- Advance scientific and clinical knowledge for immunology in rheumatologic diseases
- Incorporate new trial, scientific and digital methodologies
- Pro-actively progress study execution
- Oversee the execution of clinical studies in compliance with internal SOPs, GCP, ICH guidelines and other regulations
- Review documents supporting clinical development such as Investigatorโs brochure, regulatory documents for IND / CTA, clinical sections of integrated development plans, and submission dossiers for regulatory approval
- Engage with health authorities (contribute to health authority submissions and timely response to regulatory reviews)
- Serve as a medical expert and provide strategic input to early-stage programs
- Collaborate with external experts, key opinion leaders, and investigators to advance clinical research
- Represent Sanofi at scientific conferences and regulatory meetings
Qualifications
- MD or MD/PhD in a relevant scientific discipline with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization
- Experience/enthusiasm in advancing assets from discovery into clinical development (experience in pharma or academia)
- Experience in novel approaches to translational medicine
- Deep scientific, technical and clinical knowledge in immunologic/rheumatologic diseases
- Expertise in autoimmune and inflammatory diseases, particularly in rheumatology
- Problem solving skills
- Understand and stay updated with pre-clinical, clinical pharmacology and clinical data relevant to the molecule and therapeutic area
- Strong leadership with the ability to influence and collaborate effectively in a matrix environment
- Excellent communication and presentation skills to articulate complex scientific concepts to diverse audiences
- Proven track record of scientific publications and presentations at international conferences
Skills
- Clinical development planning and execution
- Cross-functional team leadership
- Regulatory strategy and health authority engagement
- Translational medicine and novel methodologies
- Immunology and rheumatology expertise
- Excellent written and verbal communication
- Strategic thinking and problem solving
Education
- MD or MD/PhD required (as noted above)