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Full-time

Temporary Clinical Research Associate

Competitive

Boston, MAScience & PharmaceuticalPosted 21d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Location

Boston, MA

Posted

21 days ago

Job description

WHOOP is on a mission to unlock human performance and healthspan. As a Temporary Clinical Research Associate, you will provide monitoring and clinical operations support across WHOOP’s portfolio of clinical research studies, ensuring compliance with protocols and regulations.

Responsibilities

Conduct remote and onsite monitoring activities for assigned studies, including Site Initiation Visits, Interim Monitoring Visits, Closeout Visits, and other study-specific visits

Perform monitoring activities in accordance with approved protocols, monitoring plans, Good Clinical Practice, applicable regulations, and WHOOP procedures

Review informed consent documentation, participant eligibility, source documentation, case report forms, protocol adherence, safety documentation, and study data for accuracy and completeness

Prepare accurate and timely 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

Support site readiness activities, including review of essential documents, training completion, systems access, and operational preparedness

Assist with site and study team training on protocols, study procedures, documentation requirements, and clinical systems

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

Preferred

Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies

Familiarity with ISO 14155 or clinical research involving medical devices

Experience working in a sponsor, CRO, or research-site environment

Experience supporting studies related to cardiovascular health, women's health, sleep, metabolic health, or digital biomarkers

Medical-device experience

Digital-health experience

Wearable-technology experience

Remote-monitoring studies

ISO 14155 familiarity

Sponsor environment experience

CRO experience

Research-site experience

Cardiovascular health studies

Women’s health studies

Sleep studies

Metabolic health studies

Digital biomarkers studies

Company

Health and fitness wearable with continuous monitoring

Boston, Massachusetts, USA

http://www.whoop.com/

Founded in 2012

501-1000 employees

Qualifications

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

Strong attention to detail and the ability to identify and clearly document study risks, compliance concerns, and data quality issues

Strong written communication skills, including the ability to prepare clear monitoring reports and site follow-up correspondence

Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies

Familiarity with ISO 14155 or clinical research involving medical devices

Experience working in a sponsor, CRO, or research-site environment

Experience supporting studies related to cardiovascular health, women's health, sleep, metabolic health, or digital biomarkers

3+ years of experience in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.

Required skills

Clinical Research, Clinical Monitoring, Clinical Practice, Protocol Adherence, Informed Consent Documentation, Case Report Forms, Safety Documentation, Trial Master File Management, Clinical Operations Documentation, ISO 14155, Medical Device Clinical Research

Preferred skills

Glassdoor, 3.4, Boston, Massachusetts, USA, http://www.whoop.com, Late Stage, Total Funding, $989.75M, Key Investors, Collaborative Fund, SR_A, SoftBank Vision Fund, 2026-03-31, Series G· $575M, 2026-01-15, Undisclosed, 2022-06-30, Series Unknown· $10M, Leadership Team, Garrett Bastable, Chief Operating Officer, Dirk-Jan van Hameren, Chief Marketing Officer, Recent News, Medical Product Outsourcing, Former Glossier CEO Joins WHOOP as Chief Commercial Officer, 2026-10-17, STAT, https://fastcompanyme.com, 2026-10-16, Company data provided by

Experience

3+ years

Interested in this role?

Apply directly on the employer's website — it only takes a few minutes.

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