Clinical Scientist

Posted 1.3.24
Location
Boston, MA
At WHOOP, we’re on a mission to unlock human performance. WHOOP empowers users to perform at a higher level through a deeper understanding of their bodies and daily lives.
WHOOP is currently seeking a highly motivated and skilled Clinical Scientist to join our team. This vital role encompasses the design, implementation, and analysis of clinical trials. The successful candidate will play a pivotal role in maintaining the scientific integrity of our clinical studies, contributing significantly to regulatory submissions, and effectively translating clinical research into impactful medical strategies.
RESPONSIBILITIES:
  • Design and develop clinical study protocols with a focus on scientific rigor, statistical validity, and global regulatory compliance
  • Conduct statistical analysis of clinical data, interpret results, and ensure accuracy in statistical conclusions
  • Prepare clinical study reports, ensuring adherence to regulatory standards for US and international submissions
  • Collaborate with teams to oversee clinical trials, focusing on protocol adherence, timelines, and statistical analysis plans
  • Develop study materials such as case report forms, investigator brochures, and patient consent forms, compliant with global regulations
  • Draft and submit grant applications for research funding opportunities
  • Contribute to regulatory documentation, including submissions and responses to regulatory authorities in various regions
  • Support clinical product development by integrating clinical data and insights into product design and functionality
  • Participate in creating, reviewing, and approving scientific publications, presentations, and marketing materials, ensuring compliance with diverse regulatory environments
  • Liaise with key opinion leaders, investigators, and internal stakeholders to support global clinical program success
QUALIFICATIONS:
  • Advanced degree (Ph.D., PharmD, or MD) in life sciences, pharmacy, or related field, with a strong background in biostatistics or related discipline preferred
  • 3-5 years of experience in clinical research and statistical analysis in the [digital health/pharmaceutical/biotechnology] sector
  • In-depth knowledge of GCP, ICH guidelines, and US and international regulatory requirements in clinical research
  • Proven experience in clinical trial design, execution, analysis, and interpretation
  • Experience in global regulatory documentation, clinical product development, and marketing material creation
  • Proficiency in statistical software (e.g., SAS, R, SPSS)
  • Excellent analytical skills with the ability to interpret complex clinical data
  • Strong verbal and written communication skills, and the ability to work effectively in diverse team environments
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