Clinical Research Coordinator

Clinical Research Coordinator

Launch your career in clinical research with a role that offers hands-on experience in cardiology studies, direct patient interaction, and collaboration with physicians, sponsors, and healthcare professionals. This is an excellent opportunity for recent graduates interested in healthcare, research, or medicine who are looking to build valuable clinical experience while contributing to innovative cardiovascular research.

Location: Denver, CO Metro Area (Primary office in Golden with travel to Westminster, Longmont, and Louisville offices as needed)

Pay Rate: Starting at $22.00/hour, based on relevant experience

Employment Type: Temporary to hire

Schedule: M-F, 8am-5pm, with some flexibility required

Why This Role Matters

As a Research Coordinator, you'll play a key role in supporting cardiovascular clinical trials and helping bring new treatments and technologies to patients. You'll work closely with physicians, study participants, sponsors, and research teams to ensure studies are conducted accurately, ethically, and in compliance with all regulatory requirements.

What You'll Do

Screen, recruit, and support study participants throughout the clinical trial process

Coordinate study visits, protocol-related procedures, and participant follow-up care

Review and collect data from electronic medical records and study source documents

Complete informed consent processes and explain research protocols in patient-friendly language

Enter and maintain data within electronic data capture systems and study databases

Observe hospital-based procedures and surgeries to support study documentation requirements

Maintain regulatory binders, source documents, and study records in accordance with protocol requirements

Track study metrics and provide regular updates to leadership and research teams

Coordinate sponsor meetings, monitoring visits, site initiation visits, and study close-out activities

Report adverse events and ensure compliance with IRB-approved protocols and Good Clinical Practice (GCP) guidelines

What We're Looking For

A current, up-to-date resume

Bachelor's degree required

Clinical experience required; cardiovascular experience strongly preferred

Previous clinical research experience preferred

Understanding of clinical research principles, including GCP, informed consent, HIPAA, and human subject protections

Proficiency with Microsoft Office applications, including Excel

Strong communication, organizational, and problem-solving skills

Ability to work independently across multiple office locations

Experience with electronic medical records and data entry systems preferred

Valid driver's license and current auto insurance required

Strong attention to detail and ability to manage multiple priorities and deadlines

Ability to meet compliance requirements

What's In It For You

Gain valuable clinical research experience in a respected cardiovascular practice

Work alongside physicians, healthcare professionals, and industry sponsors

Develop skills in patient interaction, clinical operations, and regulatory compliance

Exposure to cutting-edge cardiovascular research and clinical trials

Opportunity to build experience for future careers in medicine, healthcare, or research

Collaborative team environment with ongoing learning opportunities

Benefits for Manpower Associates (Upon Eligibility)

Upon completion of waiting period associates are eligible for:

Medical and Prescription Drug Plans

Dental Plan

Supplemental Life Insurance

Short Term Disability Insurance

401(k)