Clinical trial assistant • longmont co
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 pr... Show more
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The average salary range is between $ 41,600 and $ 97,500 year , with the average salary hovering around $ 55,809 year .
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)
