Job description

Department:
SOM KC Cancer Center Clinical Trials
-----
Administration

Position Title:
Clinical Research Coordinator

Job Family Group:
Professional Staff

Job Description Summary:
Job Description:
The Clinical Research Coordinator (CRC) is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. The CRC will manage The University of Kansas Cancer Center clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Monitor participants' progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols.

The University of Kansas Cancer Center is the region's only National Cancer Institute-designated comprehensive cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.

The starting salary is between the minimum and midpoint of the salary range listed.

We offer a comprehensive benefits package: Health, Dental, Vision (effective day 1), employer paid life, LTD, flexible benefits plan, miscellaneous voluntary plans available, paid vacation and sick (begin accruing upon hire), paid holidays, paid discretionary day, paid bereavement leave, paid jury duty, military leave, paid parental leave, and offer generous retirement contribution. The KUCC reimburses our staff for obtaining AND maintaining their research certification and pay for one professional organization membership dues.

Required Qualifications:
Education: Associate's degree plus two years related work experience OR an equivalent combination of relevant post secondary education and work experience that equals at least 4 years.

Experience: Minimum of one year experience as a clinical research coordinator or two years healthcare experience with patient interaction or related experience. Basic understanding of regulations governing clinical research (CFR, GCP, HIPAA). Solid understanding of statutes and guidelines relevant to regulatory affairs in clinical research. Knowledgeable of study budgets, contracts and grant applications.

Skills : Excellent communication, writing, organizational and presentation skills. Ability to effectively interact with multidisciplinary teams including physicians, administrative staff. Ability to recognize competing priorities and deadlines and seek guidance in management of these where needed. Willingness to seek research certifications to further skills in the position.

Preferred Qualifications:
Research certification preferred such as Socra certification or certification eligible: Certified Clinical Research Coordinator (CCRC) or certification eligible, Certified Clinical Research Professional (CCRP) or certification eligible Collaborative Institutional Training Initiative (CITI) training certification or certification eligible.

Skills : Ability to read, speak and write Spanish preferred.

Job Duties Outlined:
Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials.

Maintain source documents and submit case report forms (CRFs) as required for clinical trials.

Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors.

Perform study procedures, as outlined in the protocol and within state and institutional scope of practice.

Assist clinical staff with sample collection, processing, handling, and shipping as outlined in the protocol and within institutional/KUMC policy.

Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies and study participants.

Prepare documentation and participate in study monitoring visits, reviews and audits. Provide written and verbal reports to Principal Investigator and Project Manager, as required.

Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.

Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures.

Attend continuing education, research and training seminars as requested by manager.

Perform other duties as assigned.

Required Documents: Must provide both:
Cover letter & Resume

The University of Kansas Medical Center and The University of Kansas Cancer Center are committed to creating and maintaining a diverse and inclusive learning and working environment, one that nurtures growth and development for all. We encourage individuals with diverse backgrounds to apply!

Employee Type:
Regular

Time Type:
Full time

Rate Type:
Salary

Pay Range:
$58,000.00 - $86,000.00
Minimum
$58,000.00
Midpoint
$72,000.00
Maximum
$86,000.00

Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Clinical-Research-Coordinator_JR003103 or go to https://careers.kumc.edu/ and search for position number JR003103.

Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered.

About KU Medical Center:
The University of Kansas Medical Centers mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu .

Benefits:
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html

KU is an EO/AAE. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability, genetic information or protected Veteran status. http://policy.ku.edu/IOA/nondiscrimination

jeid-9014d103686818418d54ea7949d00cd5

learninglandscape.com is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, learninglandscape.com provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, learninglandscape.com is the ideal place to find your next job.