Overview In this role you will support the clinical development process and collaborate with cross-functional teams to advance nutraceutical/pharmaceutical ingredients. You will help design studies, ensure GCP-compliant conduct, and translate findings into scientifically meaningful outputs such as publications or patent materials. You will engage in data interpretation, study documentation, and cross-department collaboration to drive product innovation and publication-ready material.
Responsibilities- Collaborate with the clinical development team and project leaders to design and execute studies
- Coordinate multiple clinical trials/studies and provide scientific support to researchers
- Prepare and ship trial documentation and communicate with study sites
- Assess protocol compliance with investigators and third-party facilities
- Verify data integrity using data management tools and monitoring processes
- Facilitate site recruitment, training, initiation, in-life, and close-out activities
- Engage with R&D and commercial teams across project phases
- Research novel ingredients for product innovation
- Perform statistical analysis and create tables/graphics for study reports
- Prepare scientific publications as needed
- Attend scientific conferences relevant to project needs
- Travel up to 10% and perform other duties to meet objectives
- Communicate effectively across departments in a team environment
Key requirements- Masters degree in a life science field with 4+ years of experience in nutraceutical/pharmaceutical product environments
- Experience in a clinical study related role
- Strong understanding of Good Clinical Practice (GCP) guidelines
- Strong scientific writing ability
- Self-motivated, adaptable and able to thrive in a fast-paced environment
- Ability to translate technical insights into actionable plans
- collaboration
- effective communication
- adaptability
- GCP knowledge
- data management and study monitoring tools
- statistical analysis and data visualization
