Overview As a Clinical Development Scientist, you will support the clinical development process to advance ingredient research and product development. You work with cross-functional teams to design studies, manage trials, and interpret results for patents or publications. You ensure data integrity and compliance with GCP while translating technical insights into actionable plans. This role offers exposure to project leadership, scientific communication, and opportunities to contribute to product innovation in a fast-paced environment.
Responsibilities- Collaborate with clinical development and project leaders to design and execute studies
- Plan and manage multiple clinical trials/studies with guidance, providing scientific support
- Prepare and ship site documents, and communicate with trial sites
- Assess protocol compliance by Investigator sites or contract facilities
- Verify study data using data management tools to ensure quality
- Facilitate site recruitment, training, initiation, in-life and close-out activities
- Coordinate with R&D and commercial teams across project phases
- Research novel ingredients for product innovation
- Conduct statistical analysis and produce tables/graphics for study reports
- Prepare scientific publications as needed
- Attend scientific conferences and travel up to 10% as required
Key requirements- Clinical study experience
- Strong scientific writing ability
- Understanding of GCP guidelines
- Strategic thinking with ability to translate insights into action
- Self-motivated, adaptable, thrives in a fast-paced environment
- Collaborative
- Effective communication
- Cross-functional teamwork
- GCP knowledge
- Clinical trial design and execution
- Data management and data integrity
