Senior Clinical Research Coordinator Job at University of Kansas Medical Center
University of Kansas Medical Center Kansas City, KS 66160
$65,000 - $99,000 a year
Department:
SOM KC Cancer Center Clinical Trials
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Clinical Trials Project Management
Position Title:
Senior Clinical Research Coordinator
Job Family Group:
Professional Staff
Job Description Summary:
Job Description:
The Senior Clinical Research Coordinator will work closely to support the Project Managers and Site Development Managers. The Project Management team is responsible for working collaboratively with multidisciplinary teams, consisting of Clinical Trials Office (CTO), Site Development, Regulatory Affairs, Finance staff; as well as, University of Kansas Cancer Center researchers, and hospital staff to support the selection, activation, maintenance, and termination of oncology clinical trials. This responsibility encompasses planning and executing operational aspects of clinical research programs from conception to completion, including managing deliverables, timelines, oversight of project costs, contracts and agreements.
The University of Kansas Cancer Center (KUCC) 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 for this position will be 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 generous retirement contributions.
Required Qualifications:
Education :
Bachelor's degree. Experience may be substituted for a degree on a year-for-year basis.
Research certification required such as: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or other related research certification.
Work Experience :
Four years clinical research experience.
Previous experience working in health-care related settings.
Experience with regulations, statutes, and guidelines governing clinical research (CFR, GCP, HIPAA).
Experience with study budgets, contracts and grant applications.
Experience with clinical research databases and software.
Excellent written and verbal communication skills as evidenced by application materials and interview process.
Proficient in PC operations and software applications such as MS Outlook, Windows, Excel and Word.
Preferred Qualifications:
Skills :
Strong customer service skills.
Superb attention to detail, organizational, and time management skills.
Proficient in medical terminology.
Job Duties Outlined:
Communicate project findings and priorities. Assist team members with prioritization, problem solving and resourcing.
Interact on a daily basis with clinical research staff, investigators, patients, and clinic staff demonstrating strong interpersonal skills using tact and good judgement.
Prepare agenda and minutes for assigned Disease Working Group (DWG) meetings.
Aid in multidisciplinary communication for study startup activities.
Prepare prospective trials for the Executive Resourcing Committee (ERC).
Effectively participate in project teams to accomplish organizational goals for patient accrual and study start-up timelines.
Support upper management using effective tracking tools to provide consistent and accurate project status.
Manage contractual and organizational client expectations.
Assist Program Managers with the scheduling of Site Initiation Visits (SIV).
Assist Site Development team maintaining key strategic partnerships.
Assist with the coordination, preparation and maintenance of clinical trial contract documents and study budget reports.
Attend continuing education, research and training seminars as requested by manager.
Participate in quality assurance activities by reviewing clinical data.
Coordinate closely with the Research Institute and Human Research Protection Program and have a significant working knowledge of KUMC policies and procedures.
Review and assist with editing of new protocols. Assess feasibility of research protocol including appropriate patient population, budget and specific needs for the study.
This is lead position which involves mentoring and training junior staff.
Other relevant duties as requested by the supervisor.
Required Documents:
Cover Letter and Resume/CV
Employee Type:
Regular
Time Type:
Full time
Rate Type:
Salary
Pay Range:
$65,000.00 - $99,000.00
Minimum
$65,000.00
Midpoint
$82,000.00
Maximum
$99,000.00
Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Senior-Clinical-Research-Coordinator_JR005456 or go to https://careers.kumc.edu/ and search for position number JR005456.
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-5579f3ddf7fb6e45b898baed6f4dd56b
Please Note :
www.bankofmontserrat.ms 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, www.bankofmontserrat.ms 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, Site.com is the ideal place to find your next job.
SOM KC Cancer Center Clinical Trials
-----
Clinical Trials Project Management
Position Title:
Senior Clinical Research Coordinator
Job Family Group:
Professional Staff
Job Description Summary:
Job Description:
The Senior Clinical Research Coordinator will work closely to support the Project Managers and Site Development Managers. The Project Management team is responsible for working collaboratively with multidisciplinary teams, consisting of Clinical Trials Office (CTO), Site Development, Regulatory Affairs, Finance staff; as well as, University of Kansas Cancer Center researchers, and hospital staff to support the selection, activation, maintenance, and termination of oncology clinical trials. This responsibility encompasses planning and executing operational aspects of clinical research programs from conception to completion, including managing deliverables, timelines, oversight of project costs, contracts and agreements.
The University of Kansas Cancer Center (KUCC) 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 for this position will be 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 generous retirement contributions.
Required Qualifications:
Education :
Bachelor's degree. Experience may be substituted for a degree on a year-for-year basis.
Research certification required such as: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or other related research certification.
Work Experience :
Four years clinical research experience.
Previous experience working in health-care related settings.
Experience with regulations, statutes, and guidelines governing clinical research (CFR, GCP, HIPAA).
Experience with study budgets, contracts and grant applications.
Experience with clinical research databases and software.
Excellent written and verbal communication skills as evidenced by application materials and interview process.
Proficient in PC operations and software applications such as MS Outlook, Windows, Excel and Word.
Preferred Qualifications:
Skills :
Strong customer service skills.
Superb attention to detail, organizational, and time management skills.
Proficient in medical terminology.
Job Duties Outlined:
Communicate project findings and priorities. Assist team members with prioritization, problem solving and resourcing.
Interact on a daily basis with clinical research staff, investigators, patients, and clinic staff demonstrating strong interpersonal skills using tact and good judgement.
Prepare agenda and minutes for assigned Disease Working Group (DWG) meetings.
Aid in multidisciplinary communication for study startup activities.
Prepare prospective trials for the Executive Resourcing Committee (ERC).
Effectively participate in project teams to accomplish organizational goals for patient accrual and study start-up timelines.
Support upper management using effective tracking tools to provide consistent and accurate project status.
Manage contractual and organizational client expectations.
Assist Program Managers with the scheduling of Site Initiation Visits (SIV).
Assist Site Development team maintaining key strategic partnerships.
Assist with the coordination, preparation and maintenance of clinical trial contract documents and study budget reports.
Attend continuing education, research and training seminars as requested by manager.
Participate in quality assurance activities by reviewing clinical data.
Coordinate closely with the Research Institute and Human Research Protection Program and have a significant working knowledge of KUMC policies and procedures.
Review and assist with editing of new protocols. Assess feasibility of research protocol including appropriate patient population, budget and specific needs for the study.
This is lead position which involves mentoring and training junior staff.
Other relevant duties as requested by the supervisor.
Required Documents:
Cover Letter and Resume/CV
Employee Type:
Regular
Time Type:
Full time
Rate Type:
Salary
Pay Range:
$65,000.00 - $99,000.00
Minimum
$65,000.00
Midpoint
$82,000.00
Maximum
$99,000.00
Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Senior-Clinical-Research-Coordinator_JR005456 or go to https://careers.kumc.edu/ and search for position number JR005456.
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-5579f3ddf7fb6e45b898baed6f4dd56b
Please Note :
www.bankofmontserrat.ms 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, www.bankofmontserrat.ms 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, Site.com is the ideal place to find your next job.