Clinical Research Coordinator - Cancer Center
Job Overview
Employment Type
Full-time
Compensation
Salary
Range $60,800.00 - $91,200.00
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Vision Insurance
Paid Time Off
Paid holidays
Retirement Plan
Life insurance
Job Description
The University of Kansas Medical Center (KU Medical Center) is a premier academic health sciences center dedicated to educating exceptional healthcare professionals, advancing health science through cutting-edge research, and providing compassionate, state-of-the-art patient care. It is composed of renowned schools of Medicine, Nursing, and Health Professions, delivering undergraduate, graduate, professional, postdoctoral, and continuing education programs. KU Medical Center is deeply committed to working with communities across every Kansas county to improve the health and well-being of Kansans. It is also home to the University of Kansas Cancer Center, which holds the distinguished National Cancer Institute designation as a Comprehensive Cancer Center, being one of only 57 in the country to have such status. This recognition highlights its cutting-edge clinical trials, promising therapies, and world-class research aimed at combating cancer effectively.
The position of Clinical Research Coordinator within the KU Cancer Center plays a pivotal role in supporting clinical research efforts aimed at improving cancer treatments and patient outcomes. As a Clinical Research Coordinator, you will be part of a multidisciplinary and collaborative team involving researchers, clinicians, and hospital staff. Your primary responsibility will be to recruit, screen, and educate potential patients on relevant clinical trials, ensuring they meet eligibility criteria. This role requires managing complex activities involved in collecting, compiling, documenting, and analyzing clinical research data while maintaining compliance with federal regulations and institutional policies.
In this patient-facing, full-time role, you will actively monitor clinical trial participants’ progress and meticulously document any adverse events. You will ensure data accuracy and integrity through timely submission of case report forms and support clinical staff with sample collection and processing. Your responsibilities will extend to coordinating logistics related to study supplies and budget tracking as well as preparing for and participating in study monitoring visits, audits, and quality assurance activities. Working closely with principal investigators, you will provide updates and reports, continually advancing research operations. The position offers a competitive salary range from approximately $60,800 to $91,200 per year, reflective of experience and qualifications, with an excellent comprehensive benefits package starting from day one, including health, dental, and vision insurance among others.
This role offers an excellent career opportunity for individuals passionate about clinical research and oncology. It requires a detail-oriented mindset, strong organizational and communication skills, and the ability to multitask in a fast-paced environment. The Clinical Research Coordinator will gain valuable experience in clinical trial management, regulatory compliance, and collaborative research efforts at a nationally recognized cancer center dedicated to pioneering novel cancer therapies and improving patient care. The role demands a 100% onsite commitment due to its interactive and patient-centric nature, allowing you to make a tangible impact in cancer research and clinical treatment advancement.
The position of Clinical Research Coordinator within the KU Cancer Center plays a pivotal role in supporting clinical research efforts aimed at improving cancer treatments and patient outcomes. As a Clinical Research Coordinator, you will be part of a multidisciplinary and collaborative team involving researchers, clinicians, and hospital staff. Your primary responsibility will be to recruit, screen, and educate potential patients on relevant clinical trials, ensuring they meet eligibility criteria. This role requires managing complex activities involved in collecting, compiling, documenting, and analyzing clinical research data while maintaining compliance with federal regulations and institutional policies.
In this patient-facing, full-time role, you will actively monitor clinical trial participants’ progress and meticulously document any adverse events. You will ensure data accuracy and integrity through timely submission of case report forms and support clinical staff with sample collection and processing. Your responsibilities will extend to coordinating logistics related to study supplies and budget tracking as well as preparing for and participating in study monitoring visits, audits, and quality assurance activities. Working closely with principal investigators, you will provide updates and reports, continually advancing research operations. The position offers a competitive salary range from approximately $60,800 to $91,200 per year, reflective of experience and qualifications, with an excellent comprehensive benefits package starting from day one, including health, dental, and vision insurance among others.
This role offers an excellent career opportunity for individuals passionate about clinical research and oncology. It requires a detail-oriented mindset, strong organizational and communication skills, and the ability to multitask in a fast-paced environment. The Clinical Research Coordinator will gain valuable experience in clinical trial management, regulatory compliance, and collaborative research efforts at a nationally recognized cancer center dedicated to pioneering novel cancer therapies and improving patient care. The role demands a 100% onsite commitment due to its interactive and patient-centric nature, allowing you to make a tangible impact in cancer research and clinical treatment advancement.
Job Requirements
- Four years of relevant work experience or education substitution
- Experience with clinical research regulations such as CFR, GCP, and HIPAA
- Knowledge of regulatory affairs in clinical research
- Experience with study budgets, contracts, and grant applications
- Proficiency in MS Office
- Attention to detail
- Strong time management skills
- Effective interpersonal and communication skills
- Ability to work onsite full time
- Commitment to patient-facing role
Job Qualifications
- Bachelor's degree preferred
- Four years of relevant work experience or education substitution
- Knowledge of CFR, GCP, and HIPAA regulations
- Familiarity with regulatory affairs, study budgets, contracts, and grant applications
- Proficiency with MS Office products
- Strong attention to detail
- Excellent time management and organizational skills
- Good interpersonal and communication skills
- Ability to multitask effectively
Job Duties
- Recruit and educate potential patients and evaluate patient eligibility for clinical trials
- Maintain source documents and submit case report forms for clinical trials
- Recognize and report adverse events and serious adverse events to the Principal Investigator, FDA, and sponsors
- Perform study procedures as outlined in protocols and within scope of practice
- Assist clinical staff with phlebotomy and sample collection, processing, handling, and shipping
- Ensure study supplies are maintained and track study expenditures
- Prepare documentation and participate in study monitoring visits, reviews, and audits
- Participate in quality assurance activities ensuring compliance with guidelines
- Collaborate with Research Institute and Human Research Protection Program
- Attend continuing education, research and training seminars as requested by management
Job Criteria
Experience
Mid Level (3-7 years)
Job Location
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