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Lead Clinical Research Scientist

WHOOP is an advanced health and fitness wearable on a mission to unlock human performance. WHOOP empowers its members to improve their health and perform at a higher level through a deeper understanding of their bodies and daily lives.


As the Lead Clinical Research Scientist, you will drive the end-to-end development of clinical strategy and scientific evidence across a portfolio of innovative health features spanning both regulated and unregulated domains. This role combines subject matter expertise, regulatory-savvy strategy, and hands-on leadership in clinical trial design, data analysis, and cross-functional alignment.


You will manage and mentor a growing team of Clinical Scientists, lead high-impact clinical studies, and help WHOOP generate the evidence required for product development, regulatory submissions, and long-term member trust. This role is ideal for someone with strong clinical acumen, technical fluency, and deep experience in digital health, medical device development, or pharmaceutical trials.


RESPONSIBILITIES:
  • Lead clinical strategy across multiple initiatives, from feature ideation to post-market activities.
  • Serve as a scientific and clinical subject matter expert in internal discussions and external engagements (e.g., FDA, Notified Bodies).
  • Shape evidence generation plans to support regulatory submissions and business priorities.
  • Oversee clinical data generation, ensuring adherence to CDISC and regulatory standards.
  • Develop and review documentation including study protocols, CRFs, SAPs, and regulatory submissions (e.g., CERs, CSRs, 510(k) packages).
  • Maintain and grow collaborative relationships with regulatory agencies (e.g., FDA, EMA), including pre-submission meetings and ongoing communications.
  • Partner with Regulatory and Quality teams to ensure compliance with ICH-GCP, ISO 14155, and FDA regulations.
  • Manage and mentor Clinical Scientists, fostering high-quality scientific execution and career development.
  • Conduct technical reviews and quality control of scientific documentation and statistical deliverables.
  • Support hiring and onboarding efforts to build a well-rounded clinical function.
  • Work closely with product, data science, engineering, and legal teams to ensure clinical and scientific input throughout the product lifecycle.
  • Partner with data teams to analyze and interpret clinical and real-world datasets.


QUALIFICATIONS:
  • Advanced degree (Ph.D., MD, or PharmD) in life sciences, public health, or a related field.
  • 7+ years of experience in clinical research or clinical science, including at least 2 years of direct people management or team leadership.
  • Demonstrated experience leading full-cycle clinical trials or regulated studies in digital health, medical devices (esp. SaMD), or pharmaceuticals.
  • Led or contributed to SaMD regulatory submissions (e.g., 510(k), De Novo, CE Mark)
  • Strong knowledge of clinical data standards and tools - CDISC (SDTM/ADaM), R, SAS, and/or Python.
  • Deep understanding of FDA and international regulatory pathways and documentation requirements.
  • Proven ability to build cross-functional relationships and communicate clearly across technical and non-technical teams.
  • Experience mentoring junior team members and conducting quality checks on clinical and regulatory deliverables.
  • Nice to have: Prior experience working at or closely with a regulatory agency (e.g., FDA), or a strong history of successful regulatory interactions.
  • Nice to have: Background in both CRO and sponsor-side clinical roles.
  • Nice to have: Familiarity with software validation processes and SaMD evidence generation.


This role is based in the WHOOP office located in Boston, MA. The successful candidate must be prepared to relocate if necessary to work out of the Boston, MA office. 


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.  It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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What You Should Know About Lead Clinical Research Scientist, WHOOP

WHOOP, a pioneer in advanced health and fitness wearables, is on a mission to revolutionize human performance through deeper insights into health and daily lives. We are excited to invite applications for the position of Lead Clinical Research Scientist. This critical role involves spearheading the development of clinical strategies and generating scientific evidence for our cutting-edge health features, both in regulated and unregulated spaces. As the Lead Clinical Research Scientist, you will leverage your expertise in clinical trial design and data analysis, while also managing and mentoring a dynamic team of Clinical Scientists. You’ll lead impactful clinical studies that help ensure WHOOP’s product innovations are backed by solid evidence for regulatory submissions and member trust. If you have a robust background in digital health, medical devices, or pharmaceuticals, combined with a passion for improving health outcomes, then this could be your next great opportunity. You'll collaborate closely with cross-functional teams, maintain sustainable relationships with regulatory agencies, and oversee compliance with all relevant standards. Bring your knowledge, leadership skills, and commitment to scientific excellence to WHOOP in Boston, MA, where together we will take human performance to the next level.

Frequently Asked Questions (FAQs) for Lead Clinical Research Scientist Role at WHOOP
What are the key responsibilities of a Lead Clinical Research Scientist at WHOOP?

As a Lead Clinical Research Scientist at WHOOP, you will be at the forefront of clinical strategy across various initiatives—from ideation to post-market activities. Responsibilities include serving as a clinical expert in discussions with regulatory bodies like the FDA, overseeing data generation, maintaining compliance with CDISC standards, and mentoring a talented team of Clinical Scientists. You will also partner with other teams to ensure that scientific input is seamlessly integrated throughout the product lifecycle.

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What qualifications are necessary to become a Lead Clinical Research Scientist at WHOOP?

To qualify for the Lead Clinical Research Scientist position at WHOOP, candidates should possess an advanced degree (Ph.D., MD, or PharmD) in life sciences or a related field, along with over seven years of experience in clinical research. Experience in leading full-cycle clinical trials, particularly in regulated environments such as digital health, is essential. Additionally, a strong command of clinical data standards and regulatory pathways is critical.

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How does WHOOP support the career development of its Clinical Scientists?

WHOOP emphasizes career development for its Clinical Scientists by fostering an environment of mentorship and growth. As a Lead Clinical Research Scientist, you will manage and guide a team, ensuring they receive feedback, support, and opportunities for professional advancement. WHOOP's commitment to individual development ensures that each scientist can thrive in their role and enhance their skill sets.

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What is the significance of regulatory submissions for a Lead Clinical Research Scientist at WHOOP?

Regulatory submissions play a vital role for the Lead Clinical Research Scientist at WHOOP, as they ensure that the company's innovative health solutions are compliant with necessary legal and safety standards. This position requires crafting documentation for submissions—including 510(k) packages and clinical evaluation reports—while shaping evidence generation plans that align both with product development needs and regulatory priorities.

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What tools and knowledge are essential for a Lead Clinical Research Scientist at WHOOP?

Being a successful Lead Clinical Research Scientist at WHOOP requires proficiency in clinical data tools such as R, SAS, or Python, alongside a deep understanding of clinical data standards like CDISC. Knowledge of FDA regulations and experience navigating different regulatory pathways adds significant value, enabling you to effectively contribute to WHOOP’s mission of transforming human performance.

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Common Interview Questions for Lead Clinical Research Scientist
Can you explain your experience in leading clinical trials relevant to the Lead Clinical Research Scientist role?

When answering this question, showcase specific trials you've led, focusing on your role in their design, execution, and outcomes. Highlight any challenges faced and how you overcame them, emphasizing your strategic thinking and leadership skills.

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How do you ensure compliance with regulatory standards in clinical studies?

One effective approach is to maintain up-to-date knowledge of regulatory requirements and involving cross-functional teams in the development of study protocols. Discuss specific compliance strategies you’ve implemented, and how you’ve tracked and audited study adherence to quality standards.

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Describe a time you had to mentor a junior team member. What was your approach?

Consider sharing a specific example that illustrates your mentoring style. Focus on how you set clear expectations, provided constructive feedback, and fostered an open environment where the individual felt supported and empowered to ask questions.

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What steps do you take to collaborate effectively with regulatory agencies like the FDA?

Detail your strategy for maintaining clear and open lines of communication, including how you prepare for meetings and what data you provide to support your discussions. Emphasize any successful engagements you've had that led to positive outcomes.

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How do you approach clinical data analysis for large datasets?

Discuss your experience using statistical tools like R or SAS to analyze clinical data. Mention how you ensure accuracy and validity in your analyses, and how you translate complex data findings into actionable insights for stakeholders.

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What are the most important qualities of a Lead Clinical Research Scientist?

Talk about qualities such as leadership, analytical thinking, attention to detail, and strong communication skills. Provide examples of how you’ve demonstrated these qualities in previous roles, reinforcing their importance in collaborative clinical research environments.

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Can you discuss your experience with software validation processes?

If applicable, speak to any specific frameworks you've worked within for software validation. Highlight your understanding of the processes necessary to ensure compliance for Software as a Medical Device (SaMD) and any notable projects you've contributed to.

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In what ways do you handle challenges in clinical trial designs?

Use this opportunity to discuss your problem-solving abilities by providing examples of challenges faced in past studies, how you addressed those issues, and what the outcomes were. Emphasize creative and strategic solutions.

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Why is mentorship important in clinical research settings?

Mentorship is key to developing the next generation of clinical scientists, ensuring knowledge transfer and fostering innovation. Discuss your commitment to mentorship by sharing experiences where you’ve contributed to the professional growth of others.

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What motivated you to apply for the Lead Clinical Research Scientist position at WHOOP?

Express your passion for pursuing health innovation and how WHOOP’s mission resonates with your professional values. Be specific about how your experience aligns with the needs of the position and how you envision contributing to the team.

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Our mission at WHOOP is to unlock human performance. We believe that every individual has an inner potential that can be enhanced through continuous monitoring. As such we've built a system across hardware, software, and analytics designed to coll...

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DATE POSTED
April 24, 2025

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