Clinical
Vanda Pharmaceuticals
August 19, 2026
Remote friendly (Washington, DC)
United States
Other
Primary 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
Qualifications:
- Undergraduate or graduate degree in Biology, Medicine, Health Sciences or related field, with strong academic record
- Exposure to basic sciences/clinical research
- Excellent oral and written communication skills, self-motivation, and ability to adapt within a dynamic environment
Benefits:
- Health insurance, unlimited paid time off, parental leave, 401k matching program, incentive compensation
Application instructions:
- If you reside in a state or locality with enacted pay transparency laws, you are entitled to request and receive additional details regarding compensation and benefits. For assistance, contact 202-524-8238 between 8:00 AM and 5:30 PM ET, Monday through Friday.
- 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
Qualifications:
- Undergraduate or graduate degree in Biology, Medicine, Health Sciences or related field, with strong academic record
- Exposure to basic sciences/clinical research
- Excellent oral and written communication skills, self-motivation, and ability to adapt within a dynamic environment
Benefits:
- Health insurance, unlimited paid time off, parental leave, 401k matching program, incentive compensation
Application instructions:
- If you reside in a state or locality with enacted pay transparency laws, you are entitled to request and receive additional details regarding compensation and benefits. For assistance, contact 202-524-8238 between 8:00 AM and 5:30 PM ET, Monday through Friday.