Research Coordinator (Career Transition)

Cardiovascular Associates of America•Davenport, IA

13d•Onsite

About The Position

Clinical Research Coordinator (Entry-Level / Career Transition Opportunity) Location: Davenport, IA (On-Site) Organization: Cardiovascular Medicine (CVM), part of Cardiovascular Associates of America (CVAUSA) 🚑 No Nights. No Weekends. No On-Call. Looking for a more predictable schedule and a new career path in healthcare? This is a unique opportunity to transition into clinical research—where you can make a meaningful impact without the burnout of traditional clinical roles. 💙 Start a Career in Clinical Research—Right Here in the Quad Cities Are you passionate about healthcare, science, or patient care—but looking for a new path with growth and purpose? Join Cardiovascular Medicine (CVM)—a leading cardiovascular practice serving patients across Iowa, Illinois, and the Midwest for over 45 years. As part of CVAUSA’s national research network, CVM is bringing clinical trials directly into the community—giving patients access to new and innovative treatments close to home. We’re looking for motivated individuals who are excited to learn and grow—no prior research experience needed. 💡 What is Clinical Research? Clinical research is how new medications, devices, and therapies are developed and tested. 🚀 What You’ll Do As a Clinical Research Coordinator, you’ll be part of a team that: Helps bring new cardiovascular treatments to patients Ensures studies are conducted safely and ethically Works closely with patients, physicians, and research sponsors This role blends patient care, science, and coordination—making it both meaningful and intellectually engaging. 🎯 Who This Role Is Perfect For We are intentionally opening this opportunity to individuals looking to grow into a new career, including: EMTs or Paramedics seeking a more structured, long-term path Medical Assistants (MAs) with strong clinical and administrative skills Phlebotomists, Radiology Techs, or other healthcare technicians Recent graduates in biology, health sciences, or related fields Healthcare professionals interested in transitioning into research If you are someone who: Enjoys working with patients while managing details behind the scenes Is curious and enjoys learning new skills Takes initiative and wants to grow professionally Is comfortable with technology and organization …this could be a great next step. 🛠️ Key Responsibilities You will be trained to: Screen patients for clinical trial eligibility Coordinate and schedule study visits within a busy cardiovascular practice Support patient visits (vitals, ECGs, specimen collection as applicable) Educate patients on clinical trials and assist with informed consent (once trained) Manage study documentation and data entry (CTMS, EHR, regulatory systems) Ensure compliance with study protocols and regulatory standards (GCP) Collaborate with physicians and care teams on active clinical trials This is a hands-on, fully on-site role in Davenport, working within a high-volume cardiovascular practice. ⭐ Why This Role Is Unique Opportunities in clinical research are limited in this region—making this a rare chance to enter a high-growth field without relocating. In this role, you will: Work alongside leading cardiovascular specialists Gain exposure to advanced diagnostics and procedures Be part of a team bringing research and innovation to the Quad Cities Help expand access to clinical trials for local patients

Requirements

Strong attention to detail and organizational skills
Excellent communication and interpersonal skills
Willingness to learn and take initiative
Comfort with technology and systems

Nice To Haves

Clinical or patient-facing experience
Background in healthcare or a science-related field
Bachelor’s degree (science or health-related preferred)

Responsibilities

Screen patients for clinical trial eligibility
Coordinate and schedule study visits within a busy cardiovascular practice
Support patient visits (vitals, ECGs, specimen collection as applicable)
Educate patients on clinical trials and assist with informed consent (once trained)
Manage study documentation and data entry (CTMS, EHR, regulatory systems)
Ensure compliance with study protocols and regulatory standards (GCP)
Collaborate with physicians and care teams on active clinical trials