Drimva

Whoop

Temporary Clinical Research Coordinator

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

Experience
2+ years in a stated research area, including at least 1 year in coordination, participant-facing research, or similar study operations.
Education
Bachelor’s degree in life sciences, public health, psychology, nursing, clinical research, or a related field, or equivalent relevant experience.

About the job

Provides operational support for clinical research studies from startup through participant recruitment, study conduct, data collection, and closeout.

What you'll do

  • Coordinate study workflows, systems, participant recruitment and enrollment, visits, and team training.
  • Maintain study documentation and trackers; review records and help resolve data queries and discrepancies.
  • Escalate participant concerns, protocol deviations, safety information, and operational risks; support study closeout.

What they ask for

  • Bachelor’s degree in a related field, or equivalent relevant experience.
  • 2+ years supporting clinical research, healthcare research, academic research, or human-subject studies.
  • At least 1 year performing clinical research coordination, participant-facing research, or similar study operations responsibilities.
  • Working knowledge of Good Clinical Practice and applicable human-subject research requirements.

Nice to have

  • Experience with medical-device, digital-health, wearable-technology, or remote-monitoring studies.
  • Experience with decentralized, virtual, hybrid, or site-based participant research; FDA-regulated research or ISO 14155 is also desired.

Pay

$34/hr (hourly pay rate)

Tools

electronic data capture, participant management, scheduling, compensation platforms, Trial Master File

Model-written summary · the original posting is authoritative

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