Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Essential Medical Research, LLC

Clinical Research Coordinator

Career Insights for Clinical Research Coordinator

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Kansas data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.

$112,236 / year median in Kansas

+14% projected growth

Explore Career

Job Description

Clinical Research Coordinator Essential Medical Research, LLC Overland Park, KS Job Details Full-time $45,000 - $65,000 a year 3 hours ago Benefits Health insurance Paid time off Flexible schedule Qualifications Teamwork Microsoft Excel Word embeddings Attention to detail Patient care Medical Assisting Patient interaction Productivity software
Full Job Description Job Summary :
We are seeking a detail-oriented and dedicated Clinical Research Coordinator (CRC) to join our team. The CRC will oversee and manage clinical research trials, ensuring compliance with regulatory requirements, study protocols, and organizational standards. The role involves close collaboration with physicians, patients, sponsors, and other stakeholders to advance medical treatments.
Key Responsibilities :
Study Coordination :
Manage day-to-day operations of assigned clinical research studies. Ensure compliance with study protocols, regulatory guidelines, and ethical standards.
Participant Management :
Screen, recruit, and enroll study participants in accordance with inclusion/exclusion criteria. Obtain informed consent and maintain clear communication with participants throughout the study.
Data Collection and Documentation :
Conduct patient visits (Lab draws / EKG's/ conduct patient questionnaires, record, and manage accurate clinical data in electronic or paper-based case report forms (CRFs). Ensure timely reporting of adverse events and deviations to study sponsors.
Regulatory Compliance :
Prepare and maintain regulatory documents, including Institutional Review Board (IRB) submissions. Conduct study audits and ensure adherence to Good Clinical Practice (GCP) guidelines.
Collaboration and Communication :
Act as a liaison between study sponsors, investigators, clinical staff, and participants. Schedule study visits, coordinate logistics, and facilitate effective communication.
Qualifications :
Degree in a health-related field (e.g., MA/ LPN/ Nursing, Biology, Public Health). Minimum of 2 years of experience in health care related field. Proficient in Microsoft Office Suite (Word/One Note/Excel).
Key Competencies :
Strong organizational and time-management skills. Excellent interpersonal and communication abilities. Attention to detail and commitment to maintaining data integrity. Ability to handle sensitive information with confidentiality. Problem-solving skills and adaptability to dynamic work environments.
Benefits :
Competitive salary and performance-based incentives. Comprehensive health and wellness benefits. Opportunities for professional growth and continuing education. Collaborative and inclusive work environment. How to
Apply :
Submit your resume and a cover letter to: Jennifer Cleveland Include "Clinical Research Coordinator Application" in the subject line. Interested in joining a team that contributes to groundbreaking research that advances healthcare for current all future generations?
Job Type:
Full-time Pay:
$45,000.00 - $65,000.00 per year
Benefits:
Flexible schedule Health insurance Paid time off
Work Location:
In person