RESPONSIBILITIES:
- Study Design & Protocol Development: Lead the design and development of clinical trial protocols, ensuring they align with clinical and regulatory objectives. Conduct literature searches to inform study design and statistical methodologies.
- Data Analysis & Statistical Interpretation: Use advanced statistical tools (R, Python, Stata) to analyze clinical data, interpret results, and generate actionable insights. Provide clear explanations of data trends and their implications on study outcomes.
- Literature Review & Evidence Synthesis: Conduct comprehensive literature reviews to inform study design and analysis, and integrate findings from external studies with WHOOP data.
- Data Integrity & Quality: Ensure the accuracy and integrity of clinical data by implementing robust quality control measures throughout the study lifecycle.
- Explaining Findings: Communicate findings in clear, actionable terms to clinical and product teams. Create detailed reports that translate statistical analyses into meaningful business and clinical insights.
- Report Writing & Regulatory Submission: Contribute to the development of Clinical Study Reports (CSR), publications, and regulatory submissions, ensuring accurate and regulatory-compliant documentation of findings.
- Cross-Functional Collaboration: Work with clinical teams, data managers, statisticians, and regulatory affairs to ensure the successful execution and analysis of clinical studies.
- Support HEOR Strategies: Help shape health economics and outcomes research approaches to highlight the clinical and real-world value of offerings from WHOOP.
- Publication & Presentation: Lead the preparation of manuscripts, abstracts, and presentations for internal stakeholders, scientific conferences, and peer-reviewed journals.
QUALIFICATIONS:
- Bachelor’s degree in Life Sciences, Biostatistics, Clinical Research, or a related field (Master’s or PhD preferred).
- 3+ years of experience in clinical research, data analysis, or a related field within the pharmaceutical, biotech, or medical device industries.
- Proficiency in statistical software (e.g., R, SAS) and data management platforms such as Snowflake.
- Strong understanding of FDA regulations, ICH-GCP, and clinical trial design.
- Experience in protocol development, clinical data analysis, writing clinical study reports and HEOR research.
- Demonstrated ability to perform comprehensive literature reviews and integrate findings with data analysis.
- Excellent analytical and problem-solving skills with the ability to explain complex datasets and present clear findings.
- Strong written and verbal communication skills for collaboration and presentations across multidisciplinary teams.
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What We Do
At WHOOP, we’re on a mission to unlock human performance. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives. Our wearable device and performance optimization platform has been adopted by many of the world's greatest athletes and consumers alike.
Why Work With Us
At WHOOP, we’re focused on building an inclusive and equitable team with a strong sense of belonging for everyone—increasing representation in every way as our team grows. We believe that our differences are our source of strength—so much so it’s one of our core values.
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