Regional Clinical Research Associate

🕒 May 27

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $105k - $115k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Teleflex

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $275k Venture Round on 2010-01

Healthcare Insurance • Medical Devices • Pharmaceuticals

Teleflex is a global provider of innovative medical devices and solutions, dedicated to supporting healthcare professionals and enhancing patient care. With a diverse portfolio that includes products for anesthesia, emergency medicine, interventional cardiology, and more, Teleflex aims to improve the health and quality of lives. The company emphasizes its commitment to education and customer support in the healthcare sector.

📋 Description

• Conduct assigned monitoring activities in accordance with Teleflex procedures and applicable regulations • Responsible for all monitoring activities for assigned clinical studies • Scheduling and conducting monitoring activities onsite or remote within specified timelines • Identification of data discrepancies and compliance concerns • Present findings to site research staff • Works collaboratively with Research Coordinators and Investigators • Prepares for monitoring visits and escalates significant findings • Serves as a resource to site staff • Trains and mentors Teleflex personnel on monitoring procedures • Completes monitoring visit reports and action items • Assists with team, department, and study-related projects

🎯 Requirements

• Bachelor's or Graduate degree in life sciences, nursing, or other health-related disciplines • Minimum five years as a CRA in the medical device or pharmaceutical industry or with a CRO • Demonstrated aptitude and knowledge in relevant therapeutic area • Vascular Interventional Cardiology is strongly preferred • Experience conducting monitoring activities for first in human, investigational device exemption, post-approval and/or post-market studies • Strong compliance focus and understanding of current GCP/ICH guidelines and FDA regulations • Current certification as a Certified Clinical Research Associate (CCRA) or current Certified Clinical Research Professional (CCRP) • Strong knowledge of medical terminology • Ability to work independently in a regional area with minimal supervision • Excellent organizational and problem-solving skills • Excellent interpersonal skills • Ability to interact constructively in communication of adherence to protocol and regulatory requirements

🏖️ Benefits

• medical, prescription drug, dental and vision insurance • flexible spending accounts • participation in 401(k) savings plan • various paid time off benefits, such as PTO, short- and long-term disability and parental leave