Remote Clinical Research Associate – 6-Month Contract

WHOOP; Boston (MA); On-site; USD 52,000 - 72,000; Part time

Job summary

WHOOP is seeking a Temporary Clinical Research Associate in Boston to provide monitoring and clinical operations support across its portfolio of studies. You will conduct remote and on-site visits, ensure adherence to protocols and GCP, and help with Trial Master File documentation during startup, active conduct, monitoring, and closeout.

This six-month contract offers $45 per hour and requires a life sciences degree and at least 3 years in clinical research with CRA responsibilities.

Qualifications

• Bachelor’s degree in life sciences, nursing, public health, clinical research, or equivalent experience.
• 3+ years of experience in clinical research, including at least 1 year performing CRA duties.
• Strong attention to detail and the ability to identify and clearly document study risks, compliance concerns, and data quality issues.
• Strong written communication skills for monitoring reports and site follow-ups.

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 elevate 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, and action-item resolution, final monitoring activities, and Trial Master File completion.

Skills

Clinical monitoring

Data quality

Communication

Documentation

Education

Bachelor's degree in life sciences

Job description

WHOOP is seeking a Temporary Clinical Research Associate in Boston to provide monitoring and clinical operations support across its portfolio of studies. You will conduct remote and on-site visits, ensure adherence to protocols and GCP, and help with Trial Master File documentation during startup, active conduct, monitoring, and closeout.

This six-month contract offers $45 per hour and requires a life sciences degree and at least 3 years in clinical research with CRA responsibilities.