Clinical Research Associate

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This range is provided by Impulse Dynamics. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$65,000.00/hr - $75,000.00/hr

Marlton, NJ

Hope is Here!

Impulse Dynamics (USA), Inc. is a fast‑growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac Contractility Modulation, or CCM™TM, which is delivered by the company’s Optimizer® Smart System. CCM is a first‑of‑a‑kind, proprietary, life‑changing treatment alternative for a vast population of heart failure patients across the globe. With global headquarters in Marlton, N.J., the company has additional offices in Frankfurt, Germany.

The Clinical Department is responsible for executing clinical studies inodel compliance with company standard operating procedures, good clinical practices, and applicable regulatory guidelines. The department also oversees all aspects of the study, including external vendors, and coordinates with Regulatory, Commercial, Legal, Finance, and other departments within Impulse Dynamics. In this way, the department serves as a cross‑ progeny liaison and creates a positive, collaborative team environment with an eye toward innovation and operational excellence.

You will be joining a team that is committed to meaningfully advancing the science of heart failure treatment for a global community of patients and their healthcare providers.

• Manage and organize all administrative aspects for assigned clinical trials, including creation and maintenance of site personnel contact information, mass mailings, study regulatory documents, and electronic or binder preparation for distribution.
• Assist the CTM with overseeing the monitoring visit scheduling and monitoring report review.
• Prepare CST meeting minutes.
• Act as a resource for the clinical sites and research monitors for the trial.
• Assist with training site staff who are working on the study.
• Collect regulatory documentation and ensure accuracy. Record the receipt of all key study documentation and contact site regarding missing records.
• Review various studyپرد-related tracking systems to determine and report the status of clinical trial documents.
• Collect outstanding documents by contacting the clinical trial sites or working with field monitors.
• Send notifications to the clinical trial sites regarding their IRB renewal dates.
• Maintain and audit all study‑related files in compliance with department standard operating procedures.
• Assist with the follow‑up and resolution of noted observations on audit and monitoring reports.
• Work with the clinical trial sites to ensure all required testing is forwarded to and received by the Core Laboratories.
• Ensure consistent use of study tools and training materials and compliance with standard operating procedures and policies.
• Make all the arrangements for periodic meetings, such as Physician Adjudication Committees, Data Safety Monitoring Boards, and Monthly Webcast meetings, and assist the Clinical Trial Manager with the preparation of the meetings.
• Review and approve Site Qualification Reports for new clinical trial sites.
• Train users on the EDC/case report forms and other systems that may be used (i.e., electronic regulatory Binders).
• Maintain the CTMS for site budgets and payments in accordance with the scheduled budget forанд each clinical trial site agreement. Ensure invoices are reviewed and approved on a timely basis and submitted to accounting for payment.

• 1‑2 years of clinical research experience with a bachelor’s degree and/or
• 4 years of clinical research experience with professional certification (CCRP, ACRP)
• Experience with communicating with hospital administrators, research nurses, and study coordinators.
• Working knowledge of FDA regulations, Good Clinical Practices (GCPs), and all applicable state, local, and federal regulatory requirements.
• Experience with IBM EDC, Clin Plus CTMS, Florenceisted binders, Egnyte, and/or other e‑Regulatory solutions.
• Medical device and/or heart failure clinical trials experience…