Role overview

WHOOP is seeking a Temporary Clinical Research Associate to support clinical research operations across its studies portfolio. In this six-month contract role, you will oversee monitoring activities and ensure studies meet regulatory standards and company procedures throughout their lifecycle, from startup through closeout.

Key responsibilities

Conduct remote and onsite monitoring visits for assigned studies, including site initiation, interim monitoring, and closeout activities.
Review informed consent documentation, participant eligibility records, source materials, case report forms, and study data to verify accuracy and completeness.
Prepare monitoring visit reports, follow-up communications, action-item trackers, and study status updates in a timely manner.
Identify and document protocol deviations, data quality concerns, safety issues, and compliance risks, escalating them appropriately.
Support site readiness by reviewing essential documents, confirming training completion, establishing systems access, and assessing operational preparedness.
Maintain study logs, trackers, templates, and clinical operations documentation for assigned studies.
Collaborate with internal teams including Clinical Operations, Clinical Science, Data Management, and Regulatory, as well as external research sites and vendors.
Support study closeout activities, including document reconciliation, action-item resolution, and Trial Master File completion.

Requirements

Bachelor’s degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant professional experience.
Minimum three years of experience in clinical research, with at least one year performing clinical monitoring or Clinical Research Associate responsibilities.
Strong attention to detail with demonstrated ability to identify and clearly document study risks, compliance concerns, and data quality issues.
Strong written communication skills, including ability to prepare clear monitoring reports and professional site correspondence.

What makes this role worth considering

This position offers an opportunity to contribute to clinical research at a company focused on human performance and health. You will gain exposure to diverse study types and work across multiple stages of the clinical research lifecycle while collaborating with both internal teams and external research partners.