Temporary Clinical Research Associate

Whoop
Boston
Workplace: OnsiteTemporaryUSD 45+ hourlyFunction: Research & Scientific (R&D)Experience: 3+ yearsEducation: bachelorsSkills: ["Attention to detail","Communication","Collaboration","Risk management","Independent work"]

Provide monitoring and clinical operations support across WHOOP’s portfolio of clinical research studies throughout startup, active conduct, monitoring, and closeout. Conduct remote and onsite site monitoring visits, review study and participant documentation for accuracy and completeness, prepare monitoring reports, and track/escalate deviations, quality, safety, and compliance risks. Support site readiness, training, and Trial Master File quality while collaborating with cross-functional clinical teams and external vendors.

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FursaFursa
Whoop
Whoop
1 day ago

Temporary Clinical Research Associate

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Last checked: 9 hours agoStatus: Live

Job Summary

Provide monitoring and clinical operations support across WHOOP’s portfolio of clinical research studies throughout startup, active conduct, monitoring, and closeout. Conduct remote and onsite site monitoring visits, review study and participant documentation for accuracy and completeness, prepare monitoring reports, and track/escalate deviations, quality, safety, and compliance risks. Support site readiness, training, and Trial Master File quality while collaborating with cross-functional clinical teams and external vendors.
Location: Boston
Workplace: Onsite
Employment Type: Temporary · 6 months
Job Function: Research & Scientific (R&D)
Seniority: Mid level

Key Responsibilities

  • •Conduct remote and onsite monitoring visits for assigned studies, including Site Initiation, Interim Monitoring, Closeout, and other study-specific visits.
  • •Perform monitoring activities per approved protocols, monitoring plans, Good Clinical Practice, applicable regulations, and WHOOP procedures.
  • •Review informed consent, participant eligibility, source documentation, case report forms, protocol adherence, safety documentation, and study data for accuracy and completeness.
  • •Prepare monitoring visit reports, follow-up communications, action-item trackers, and study status updates.
  • •Identify, document, track, and escalate protocol deviations, data quality concerns, safety issues, compliance risks, and operational challenges, and support site readiness, training, and study closeout/TMF activities.

Pay and Benefits

Salary: USD 45 hourly

Key Requirements

  • •Bachelor’s degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant experience.
  • •3+ years of experience in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.
  • •Ability to identify and clearly document study risks, compliance concerns, and data quality issues with strong attention to detail.
  • •Strong written communication skills to prepare monitoring reports and site follow-up correspondence.
  • •Detail-oriented, collaborative, and able to independently manage assigned monitoring activities while escalating risks or compliance concerns.
Experience:3+ yearsClinical research
Education:Bachelor's
Skills:Attention to detailCommunicationCollaborationRisk managementIndependent work

Company Brief

Whoop
Whoop designs and sells a subscription-based wearable fitness tracker and analytics platform that monitors recovery, strain, and sleep to optimize athletic performance and daily health for consumers and professional athletes.
Industry: Wearables
Company Size: Large (251 to 1,000 employees)
Growth: Scaleup
Valuation: Unicorn (USD 1B+)
Funding: Series E+
Headquarters: Boston, United States
Founded: 2012
WebsiteLinkedIn