Regional Clinical Research Associate (REMOTE)

Teleflex•Philadelphia, PA

4d•Hybrid

About The Position

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. The Interventional business unit at Teleflex offers innovative medical devices that are used to diagnose and treat coronary and peripheral vascular diseases. We place a strategic emphasis on complex coronary and peripheral interventions, vascular access, bone access, specialty biologic treatments and cardiac assist. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner™ and Turnpike™ Catheters, Ringer™ Perfusion Balloon Catheter, AC3 Optimus™ and AC3 Range™ Intra-Aortic Balloon Pumps and the OnControl™ Powered Bone Access System. Teleflex’s product portfolio now also includes Passeo™-18 Lux™ Peripheral Drug-Coated Balloon Catheter, Pantera™ Lux™ Drug-Coated Balloon Catheter, Orsiro™ Mission™ Drug-Eluting Stent, the PK Papyrus™ Covered Coronary Stent, and more. With a strong R&D footprint and pipeline, our fast-growing Interventional business unit is poised to continue the development of new technologies to serve critically ill patients for years to come. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives. The Regional Clinical Research Associate will be responsible for conducting on-site and remote monitoring visits as well as centralized monitoring in compliance with applicable regulatory standards (FDA regulations, ICH/GCP guidelines, Teleflex procedures, and IRB/EC policies and procedures) for assigned clinical studies in the field of vascular intervention or other therapeutic areas.

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.
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 specifically, 21 CFR Parts 11, 50, 54, 56, 812, and 820, ISO requirements governing medical device clinical trials.
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, including demonstrated ability to evaluate challenging situations and develop alternative solutions creatively and independently.
Excellent interpersonal skills, ability to interface and communicate effectively with internal and external collaborators including physicians, site research staff, project teams and management.
Ability to interact constructively in communication of adherence to protocol and regulatory requirements.
Responsible for adequate and reasonable home office setup including dedicated desk space to accommodate work responsibilities and Teleflex-supplied equipment.

Nice To Haves

Demonstrated aptitude and knowledge in relevant therapeutic area. Vascular Interventional Cardiology is strongly preferred.

Responsibilities

Conduct assigned monitoring activities in accordance with Teleflex procedures and applicable regulations to evaluate protocol compliance, data accuracy, and subject safety by review of regulatory documents, medical records, reported data, and device storage, if applicable.
Schedule and conduct monitoring activities onsite or remote within specified timelines and according to the risk-based monitoring plan and Teleflex procedures.
Identify data discrepancies and compliance concerns, present findings to site research staff, provide retraining if needed, provide problem-solving strategies and communicate findings to the study team and department management via escalation of issues and/or within the monitoring visit report.
Work collaboratively with Research Coordinators and Investigators to conduct monitoring visits, provide retraining, and resolve compliance concerns as appropriate.
Work cooperatively with the Teleflex Clinical Studies project team members to prepare for monitoring visits, escalate significant findings during monitoring visits, and proactively provide input on site performance.
Present findings to site staff and provide clear directions for resolution.
Review data queries with site staff to confirm understanding and resolution.
Serve as a resource to site staff between monitoring visits to provide clarification and insights regarding data queries, action items, and study visit preparation.
Train and mentor Teleflex personnel on monitoring procedures and practices.
Conduct site training and co-monitoring visits as requested by management.
Complete monitoring visit reports, action items, and monitoring visit follow-up letters per Teleflex procedures.
Assist with team, department, and study-related projects as requested, including audits, investigator meetings, training, etc.
Interface with Clinical, Regulatory, Sales, and clinical site staff as necessary to accomplish responsibilities.
Represent Teleflex in a customer facing position with the highest levels of professionalism, service, and ethics in order to strengthen the Teleflex brand and relationship with our customers.
Demonstrate initiative and critical thinking to identify and prioritize process and performance gaps and develop solutions to deliver improving results.
Exemplify continuous improvement of thought processes and focus.
Exemplify Teleflex values and ensure a fair, open, and productive climate that is engaging, ethical, and legally compliant.
Strive to work effectively across boundaries in a complex matrix environment.
Lead and participate in the process of promotional and other materials, working internally and cross-functionally to ensure materials are processed completely, based on accurate interpretation of clinical practice and data.