Clinical Research Manager



Boston, MA, USA
Posted on Tuesday, October 31, 2023
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 seeking a Clinical Research Manager to lead and guide our clinical research endeavors. The ideal candidate will have a background in clinical research, with a keen focus on digital health and regulatory submissions. This role entails staying updated on pertinent research trends, analyzing and interpreting findings, and continuously liaising with cross-functional teams, researchers, and stakeholders. Your expertise will significantly contribute to clinical evidence generating helping WHOOP further our commitment to pioneering advancements in healthcare.


  • Design, oversee, and manage clinical research activities at WHOOP
  • Assist in the preparation of clinical documentation for regulatory submissions like FDA, CE mark, among others
  • Ensure the clarity, completeness, and compliance of all clinical trial documentation
  • Analyze, interpret, and share research findings with internal teams
  • Act as a bridge between cross-functional teams, investigators, vendors, and stakeholders, ensuring efficient communication and alignment of objectives
  • Remain updated with the latest in relevant research, trends, and advancements through periodic literature searches
  • Draft grant applications to procure funding for clinical research
  • Provide regular updates to senior management and relevant stakeholders on the progress, findings, and outcomes of clinical trials
  • Foster collaborations with universities, research institutions, and other potential partners


  • A Master’s degree or higher in Clinical Research, Medicine, or a related field is preferred
  • A minimum of 5 years of experience in clinical research, protocol writing, and regulatory affairs
  • At least 3 years of experience in clinical trial management, with a notable focus on digital health or similar domains
  • Proficient knowledge of FDA and other related regulatory processes
  • Proven experience in IRB submissions and creating clinical trial documentation
  • Exceptional skills in literary research and scientific writing
  • Outstanding analytical, communication, and leadership abilities
  • Strong leadership attributes, with a knack for inspiring and steering teams
  • Superior organizational, communication, and problem-solving prowess
Interested in the role, but don’t meet every qualification? We encourage you to still apply! At WHOOP, we believe there is much more to a candidate than what is written on paper, and we value character as much as experience. As we continue to build a diverse and inclusive environment, we encourage anyone who is interested in this role to apply.
WHOOP is an Equal Opportunity Employer and participates in E-verify to determine employment eligibility