Clinical Research Coordinator (Entry-Level / Career Transition Opportunity)

Location: Davenport, IA (On-Site)
Organization: Cardiovascular Medicine (CVM), part of Cardiovascular Associates of America (CVAUSA

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

What We’re Looking For

Required

• Strong attention to detail and organizational skills

• Excellent communication and interpersonal skills

• Willingness to learn and take initiative

• Comfort with technology and systems

Preferred (Not Required)

• Clinical or patient-facing experience

• Background in healthcare or a science-related field

• Bachelor’s degree (science or health-related preferred)

What We Offer

• Predictable weekday schedule (no nights, weekends, or on-call)

• Hands-on training and mentorship in clinical research

• A clear path into a long-term, high-growth career

• Exposure to innovative cardiovascular trials and technologies

• A collaborative, mission-driven team environment

• The opportunity to make a meaningful impact on patient lives

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