Director, Clinical Science

Whoop!

Director, Clinical Science leading clinical evidence generation for WHOOP’s health features. Focusing on Software as a Medical Device (SaMD) with cross-functional team collaboration.

Posted 7/1/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesLead💰 $220,000 - $245,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical evidence strategy, regulatory submissions, and clinical study design, with a strong focus on leading cross-functional teams and influencing stakeholders. Proficient in developing and reviewing clinical deliverables and ensuring compliance with regulatory standards for medical devices and digital health technologies.

Highest-signal resume keywords

Clinical Evidence StrategyRegulatory SubmissionsClinical Study DesignStatistical Analysis PlanningTeam Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ValidationEndpoint DevelopmentEvidence Generation StrategyStatistical AnalysisClinical ResearchRegulatory RequirementsSoftware as a Medical Device (SaMD)Digital Health TechnologiesProtocol DevelopmentClinical Deliverables Review

Soft Skills

Cross-Functional CollaborationInfluencing StakeholdersCommunication Skills

Tools & Technologies

RSASPythonSQLCDISCSDTMADaM

Industry Keywords

Medical DevicesDigital BiomarkersWearable TechnologiesCardiovascular HealthRemote Patient MonitoringFDACE MarkClinical Research Organizations (CRO)

Tech Stack

Tools & technologies

PythonSQL

About the role

Key responsibilities & impact

Own the clinical evidence strategy across WHOOP’s portfolio of regulated and unregulated health features, including feasibility, validation, regulatory submission, launch, and post-market evidence generation.
Translate product concepts and algorithms into clinically meaningful indications, claims, endpoints, and evidence strategies.
Define clinical validation strategies, including study design, comparator selection, endpoint development, sample size justification, statistical analysis planning, success criteria, and evidence requirements.
Lead the design and oversight of feasibility, validation, and post-market studies supporting product development and regulatory objectives.
Lead clinical strategy and evidence development for FDA, CE Mark, and other regulatory pathways, including participation in regulatory interactions and review of clinical content for submissions.
Develop, review, and approve key clinical deliverables, including protocols, CRFs, SAPs, CSRs, CERs, and regulatory submission content.
Serve as the clinical and scientific subject matter expert for internal stakeholders, regulators, investigators, advisors, and external partners.
Partner closely with Product, Data Science, Engineering, Regulatory, Quality, Legal, and Commercial teams to ensure clinical evidence informs product, regulatory, and business decisions.
Build and lead a high-performing Clinical Science organization, including hiring, mentoring, workforce planning, and establishing scalable processes, standards, and operating models.
Communicate complex scientific, clinical, and regulatory concepts to technical and non-technical stakeholders, including executive leadership.

Requirements

What you’ll need

Advanced degree (PhD, MD, PharmD, DrPH, MPH/MS with significant relevant experience, or equivalent) in life sciences, medicine, public health, epidemiology, biostatistics, or a related field.
10+ years of experience in clinical science, clinical research, medical devices, digital health, diagnostics, pharmaceuticals, or another regulated healthcare environment.
5+ years of experience leading and developing clinical science or clinical research teams.
Demonstrated experience leading clinical evidence generation for regulated products, ideally including Software as a Medical Device (SaMD) or digital health technologies.
Deep expertise in clinical study design, endpoint development, clinical validation, statistical analysis planning, and evidence generation strategy.
Experience supporting FDA, CE Mark, or other regulatory submissions, including development of clinical evidence and participation in regulatory interactions.
Experience authoring and reviewing key clinical and regulatory deliverables, including protocols, SAPs, CSRs, CERs, and submission documentation.
Strong understanding of medical device and SaMD regulatory requirements, standards, and guidance.
Proven ability to influence cross-functional stakeholders and drive decisions across Product, Data Science, Engineering, Regulatory, Quality, and Executive Leadership.
Preferred experience with wearable technologies, digital biomarkers, cardiovascular health, women’s health, sleep, metabolic health, or remote patient monitoring.
Familiarity with machine learning-enabled medical devices, algorithm validation, and software development lifecycles preferred.
Experience interacting with FDA, Notified Bodies, auditors, or other regulatory agencies preferred.
Experience working in both sponsor and CRO environments preferred.
Working knowledge of statistical and data analysis tools such as R, SAS, Python, SQL, CDISC, SDTM, or ADaM preferred.

Benefits

Comp & perks

Competitive base salaries
Meaningful equity
Generous equity package
Health insurance
Professional development