6-Month Remote Clinical Research Associate (Contract)

WHOOP; Boston (MA); On-site; USD 51,000 - 73,000; Full time

Job summary

WHOOP is seeking a Temporary Clinical Research Associate to support monitoring and clinical operations across our studies. This six‑month, hourly position offers hands-on site and remote monitoring, with a focus on quality, compliance, and trial lifecycle activities.

The CRA will review documentation, manage site readiness, generate monitoring reports, and collaborate with cross-functional teams to address deviations and risks. Prior clinical research experience is required.

Qualifications

• Bachelor’s degree in life sciences, nursing, public health, clinical research, or equivalent.
• 3+ years of experience in clinical research, including at least 1 year monitoring/CRA.
• Strong attention to detail and ability to identify and document risks and data quality issues.
• Strong written communication for monitoring reports and site correspondence.

Responsibilities

• Perform remote and onsite monitoring visits (SIV, Interim, Closeout) for assigned studies.
• Ensure adherence to approved protocols, ICH-GCP, and study procedures.
• Review informed consent, eligibility, source data, CRFs, and safety documentation.
• Prepare monitoring visit reports, follow-up communications, and trackers.
• Identify protocol deviations, data quality concerns, safety issues, and risks.
• Support site readiness and training on protocols and documentation.
• Maintain study logs, trackers, and clinical documentation.
• Collaborate with Clinical Operations, Data Management, Regulatory, and sites.
• Assist with study closeout and Trial Master File completion.

Skills

Clinical monitoring

Documentation

Written communication

Data quality

Education

Bachelor’s degree in life sciences, nursing, public health, clinical research

Job description

WHOOP is seeking a Temporary Clinical Research Associate to support monitoring and clinical operations across our studies. This six‑month, hourly position offers hands-on site and remote monitoring, with a focus on quality, compliance, and trial lifecycle activities.

The CRA will review documentation, manage site readiness, generate monitoring reports, and collaborate with cross-functional teams to address deviations and risks. Prior clinical research experience is required.