Clinical

Vanda Pharmaceuticals

Washington, DCFresher1h agovia LinkedIn

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.

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