Sr. Clinical Research Associate


Hayward
Permanent
$100,000 - $130,000 USD a year
Clinical
PR/605468_1789159814
Sr. Clinical Research Associate

Senior CRA

USA (remote)

$100,000 - $130,000

Job Description

EPM is partnered with an innovative, late-stage medical device company developing a novel energy-based platform technology with the potential to redefine treatment approaches in high-growth therapeutic markets. Backed by strong clinical momentum, public market support, and a collaborative leadership team, the organization is advancing multiple clinical programs while building the next generation of minimally invasive solutions designed to improve patient outcomes.

This is an opportunity to join a fast-paced environment where Clinical Affairs plays a highly visible role in the success of ongoing and future studies.

Roles & Responsibilities

  • Lead site monitoring activities across multiple medical device clinical studies.
  • Support study start-up, site initiation, enrollment, monitoring, and closeout activities.
  • Review source documentation, CRFs, EDC data, device accountability records, and safety reporting documentation.
  • Ensure compliance with study protocols, FDA regulations, and ICH-GCP guidelines.
  • Prepare monitoring reports, follow-up letters, and study documentation within required timelines.
  • Support investigator meetings, site training, and cross-functional study execution activities.
  • Assist with regulatory submissions, IRB communications, and clinical study reporting.
  • Monitor site performance, enrollment progress, and data quality metrics.
  • Manage protocol deviations, adverse event reporting, and site action item follow-up.
  • Mentor junior clinical team members and contribute to process improvements.

Qualifications

  • Bachelor's degree in a scientific, clinical, or related field.
  • 5+ years of clinical research experience within medical device, biotech, or life sciences.
  • Minimum 3 years of independent CRA monitoring experience.
  • Strong knowledge of FDA regulations, ICH-GCP, and clinical trial management processes.
  • Experience with EDC, CTMS, and clinical study documentation.
  • Background supporting interventional, cardiovascular, surgical, electrophysiology, imaging, or other complex device studies preferred.
  • Excellent communication, organization, and relationship-building skills.
  • Ability to travel approximately 40%.

Benefits

  • Competitive base salary
  • Annual bonus opportunity
  • Equity participation
  • Employee Stock Purchase Program (where applicable)
  • Comprehensive medical, dental, and vision coverage
  • 401(k) retirement plan with company offerings
  • Generous PTO and company holidays
  • Flexible work environment
  • Professional development opportunities
  • High-growth company with significant career advancement potential

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