Clinical
Vanda Pharmaceuticals
Key Responsibilities
- Develop and design clinical evaluation and component studies, ensuring scientific validity and alignment with program objectives.
- Provide strategic input and hands-on development support for clinical plans and individual study protocols.
- Develop statistical analysis plans and perform preliminary and exploratory data analysis of completed clinical trials.
- Participate in the development and maintenance of clinical operating guides and ensure secure, audit-ready study file management.
- Assist in the evaluation and integration of equipment, reagents, quality control materials, and other resources utilized within clinical chemistry workflows.
- Review findings from equipment and materials evaluations with appropriate management prior to implementation.
- Support regulatory submissions and documentation by contributing clinical data analysis and study summaries.
Requirements & Tech Stack
- Exposure to basic sciences/clinical research.
Qualifications
- Undergraduate or graduate degree in Biology, Medicine, Health Sciences or related field, with strong academic record.
- Excellent oral and written communication skills.
- Self-motivation.
- Ability to adapt within a dynamic environment.
This is a full-time, onsite position requiring five days per week in the office.
The anticipated start date for the Clinical cohort is early July 2027.