Drimva

Whoop

Temporary Clinical Research Associate

Boston, MA · On-site · Full-time · Posted Aug 10, 2026

Experience
3+ years in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.
Education
Bachelor’s degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant experience.

About the job

Provides monitoring and clinical operations support across clinical research studies from startup through closeout.

What you'll do

  • Conduct remote and onsite monitoring visits and review study documentation, data, safety records, and protocol adherence.
  • Prepare monitoring reports and track or escalate study issues, risks, and compliance concerns.
  • Support site readiness, training, study documentation, and closeout, including Trial Master File completion.

What they ask for

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

Nice to have

  • Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies; familiarity with ISO 14155 or medical-device clinical research.
  • Experience in a sponsor, CRO, or research-site environment, or supporting studies in cardiovascular health, women’s health, sleep, metabolic health, or digital biomarkers.

Pay

$45/hr (hourly pay rate)

Model-written summary · the original posting is authoritative

First seen Oct 27, 2026 · Last verified Nov 5, 2026 (UTC)