Whoop
Temporary Clinical Research Associate
Boston, MA · Mid · Contract
Sponsorship not specifiedDetected 26 days ago
Clinical TrialsClinical ResearchPublic HealthResearchCommunicationGxP
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odds of building a lasting career here
33Risky
Cap-exempt (no lottery)0
Sponsors this role66
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
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from this employer's Department of Labor filings
Green-card filing pattern in this occupation
Context, not a finding about this posting: of this employer's 3 green-card filings in this occupation, 100% were for a worker who already held the job.
Files H-1B transfers
10 transfer filings in the last year, covering 10 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.
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About the role
- This is a 6 month, temporary position with an hourly pay rate of $45/hr.
Responsibilities
- Perform monitoring activities in accordance with approved protocols, monitoring plans, Good Clinical Practice, applicable regulations, and WHOOP procedures.
- Identify, document, track, and escalate protocol deviations, data quality concerns, safety issues, compliance risks, and operational challenges.
- Support site readiness activities, including review of essential documents, training completion, systems access, and operational preparedness.
- Create and maintain assigned study logs, trackers, monitoring templates, and clinical operations documentation.
- Collaborate with Clinical Operations, Clinical Science, Clinical Research Coordinators, Data Management, Regulatory, Quality, investigators, research sites, and external vendors.
- Support study closeout activities, including document reconciliation, action-item resolution, final monitoring activities, and Trial Master File completion.
- WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives.
- As a Temporary Clinical Research Associate, you will provide monitoring and clinical operations support across WHOOP's portfolio of clinical research studies.
- You will support assigned studies at various stages of the clinical lifecycle, including startup, active study conduct, monitoring, and closeout.
- You will conduct monitoring activities, review study documentation, support Trial Master File quality, track study issues, and help ensure that studies are conducted in accordance with approved protocols, Good Clinical Practice, applicable regulations, and WHOOP procedures.
Requirements
- 3+ years of experience in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.
- Strong written communication skills, including the ability to prepare clear monitoring reports and site follow-up correspondence.
- Experience working in a sponsor, CRO, or research-site environment.
- Bachelor's degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant experience.
- Strong attention to detail and the ability to identify and clearly document study risks, compliance concerns, and data quality issues.
- Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies.
- Familiarity with ISO 14155 or clinical research involving medical devices.
- Experience supporting studies related to cardiovascular health, women's health, sleep, metabolic health, or digital biomarkers.
Company info
- At WHOOP, we're on a mission to unlock human performance and healthspan.
Visa & Work Authorization
- Experience working in a sponsor, CRO, or research-site environment
This listing is sourced directly from Whoop's careers page and normalized into a canonical job model.