Director, Clinical Research Scientist
Job in
New York, New York County, New York, 10261, USA
Listing for:
Cellectis
Full Time
position
Listed on 2026-01-27
Job specializations:
-
Healthcare
Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 175000 - 225000 USD Yearly
USD
175000.00
225000.00
YEAR
Job Description & How to Apply Below
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Job Description Cellectis’ Clinical Sciences (CS) organization is seeking a highly motivated and experienced Clinical Research Scientist to support the development and execution of our proprietary UCART allogeneic CART cell therapies programs.
The Director, Clinical Research Scientist participates in the design and implementation of the development strategy and supports Clinical Science Physicians with various deliverables for effective planning and execution of their assigned program. Additionally, the candidate will work closely with the Clinical Operations Team to develop clinical development processes, templates, and potentially train and manage junior clinical research scientists.
Job Responsibilities Supports the clinical development of assigned programs and participates in designing and implementing the development strategy.Provides scientific input into the design and implementation of clinical trials, reviews and interprets clinical data, and supports activities for worldwide registration (e.g., NDA/BLA).May lead process improvement initiatives and contribute to cross-asset or cross-tumor groups depending on experience.Co-leads study team meetings with Clinical Operations.Supports clinical/medical monitoring, attends forums, and acts as a primary contact for clinical science activities, including safety reporting.Engages with external partners such as KOLs, investigators, and health authorities, alongside Clinical Sciences Physicians.Provides strategic clinical science support for studies and programs.Collaborates on protocol and ICF development, and presents to governance committees.Authors/reviews clinical narratives, develops Data Review Plans, and monitors clinical data for trends.Prepares materials for internal/external meetings, including study reports and regulatory documents.Participates in process improvements and may manage direct reports.Maintains knowledge in therapeutic areas and industry standards.Core Competencies
- Strong interpersonal and communication skills.
- Analytical and presentation skills.
- Ability to work in a fast-paced environment.
- Willingness to travel up to 20%.
Education and Experience - Advanced degree in Life Sciences or similar.
- At least 5 years of experience in clinical development, preferably in oncology/hematology and CAR T-cell therapy.
- Experience with clinical data review, protocol writing, and regulatory knowledge.
Physical Requirements - In-office 4 days/week, sedentary desk position.
Salary Range
- $175,000 - $225,000, dependent on experience.
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