Clinical Research Associate
4 weeks ago
We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at Medpace. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of our research data.
Responsibilities- Conduct site initiation, monitoring, and closeout visits to ensure compliance with regulatory requirements and study protocols.
- Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff.
- Review and verify medical records and research source documentation against case report form data.
- Communicate with site staff, including coordinators, clinical research physicians, and their site staff, to ensure good documentation practices and protocol adherence.
- Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement.
- Complete monitoring reports and follow-up letters, which includes providing summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.
- Minimum of a bachelor's degree in a health or life science-related field.
- Willing to travel approximately 60-80% nationally.
- Familiarity with Microsoft Office.
- Must hold a valid driver's license.
- Competitive pay and opportunity for significant travel bonus.
- Dynamic working environment with varying responsibilities day-to-day.
- Expansive experience in multiple therapeutic areas.
- Work within a team of therapeutic and regulatory experts.
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements.
We are an EO/AA employer and offer a comprehensive benefits package, including hybrid work-from-home options, competitive PTO packages, and employee health and wellness initiatives.
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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