Research Nurse, Cardiovascular Specialists Practice

Beacon Health System is hiringa
full-timedayshift

Research Nurse for our
Cardiovascular Specialists
Practice at Beacon Medical Groupin
Elkhart,IN
.

At Beacon Health System, you’re not just part of a team,you’re part of something bigger. Every patient interaction is a chance to lead with compassion, build trust, and create lasting impact. Here, your expertise supports healing, and your heart connects us to the communities we serve.

• Medical, Dental, & Vision Insurance through Cigna
• Life Insurance
• 403(b) Matching Retirement Fund
• Competitive Paid Time Off (PTO)
• Shift Differentials
• Employee Assistance Program (EAP)
• Tuition and Certification Reimbursement
• Clinical Ladder Program
• Local and National Discounts

As adivision of Beacon Health System,Beacon Medical Group is the largest, most comprehensive medical group in the region. Currently employing more than 250 physicians, 80 advanced practice clinicians, and representing over 35 different specialties,BMGis deeply rooted in the community it serves.

Providing comprehensive treatment witha personal touch,we'rededicated to improving health and inspiring hope throughout the region.

Asa Research Nurse,youwillreport to the Nurse Manager, Clinical Research. Is responsible for the coordination and delivery of primary care to BMG research patients entered on clinical research studies. Provides support to the patient (and caregiver) throughout the continuum of care. Completes the evaluation, documentation, research and submission of data to the sponsoring group. Utilizes in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection to ensure compliance with protocol and regulatory requirements.

• Screen and assess patient eligibility for clinical research studies through review of medical records, history, and protocol requirements.
• Coordinate the informed consent process and educate patients and caregivers on study participation, treatments, risks, and expectations.
• Manage patient enrollment, registration, randomization, and ongoing study participation from screening through follow-up.
• Monitor protocol compliance, patient safety, adverse events, medication administration, and study-related treatments, labs, and diagnostic procedures.
• Ensure timely reporting and documentation of adverse events and study activities in accordance with sponsor, IRB, FDA, and organizational requirements.
• Serve as the primary liaison between patients, physicians, sponsors, research staff, and regulatory agencies to support study execution and compliance.
• Collect, review, and submit clinical trial data accurately and within required timelines to sponsors and research organizations.
• Coordinate study monitoring visits, audits, and closeout activities while maintaining protocol documentation and regulatory records.
• Maintain investigational drug accountability records and assist with protocol medication management and distribution.
• Collaborate with physicians, nurses, and research teams to determine patient eligibility, protocol selection, and treatment planning.
• Track and monitor study participants throughout treatment and long-term follow-up periods.
• Prepare reports, maintain research documentation, and ensure adherence to departmental policies, regulatory standards, and Good Clinical Practice (GCP) guidelines.
• Participate in required training, maintain certifications, attend departmental meetings, and perform additional duties as assigned.

As a Research Nurse, this position requires a strong clinical foundation and case management knowledge to effectively…