Clinical Research Coordinator Internal Medicine (Pulmonary)
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Job Location:
Kansas City, KS - USA
Monthly Salary:
$ 58656 - 86000
Posted on:
10 days ago
Vacancies:
1 Vacancy
Job Summary
Department:
SOM KC Internal Medicine - Pulmonary Critical Care and Sleep Medicine-----
Pulmonary and Critical Care MedicinePosition Title:
Clinical Research Coordinator - Internal Medicine (Pulmonary)Job Family Group:
Professional StaffJob Description Summary:
The Clinical Research Coordinator (CRC) in the Division of Pulmonary Critical Care and Sleep Medicine is responsible for coordinating and managing clinical research studies in accordance with regulatory requirements and institutional policies. This role involves the planning implementation and oversight of research protocols ensuring compliance with FDA regulations GCP guidelines IRB approvals and HIPAA requirements. The CRC will collaborate with investigators sponsors and participants to facilitate all aspects of study conduct including subject recruitment informed consent data collection and reporting.Job Description:
Job Duties
Study Coordination & Management:
Coordinate multiple clinical research studies including investigator-initiated and industry-sponsored trials.
Develop and maintain study-specific documents including regulatory binders case report forms and data collection tools.
Ensure research protocols are conducted in accordance with IRB FDA NIH and institutional regulations.
Monitor study progress ensuring adherence to timelines and compliance with protocols.
Patient Recruitment & Enrollment:
Identify and screen eligible participants for clinical studies based on protocol inclusion/exclusion criteria.
Obtain informed consent and educate participants about study procedures risks and benefits.
Schedule study visits follow-ups and coordinate necessary clinical assessments.
Data Collection & Regulatory Compliance:
Collect and enter accurate research data into electronic data capture (EDC) systems.
Maintain compliance with Good Clinical Practice (GCP) and institutional policies.
Prepare and submit regulatory documents to IRB and sponsor organizations.
Assist in audits monitoring visits and responses to queries from regulatory agencies.
Clinical & Laboratory Responsibilities:
Coordinate sample collection processing and shipping according to study requirements.
Assist with study-related procedures such as pulmonary function tests sleep studies and vital sign monitoring under supervision.
Ensure investigational products (drugs devices) are handled per protocol and regulatory requirements.
Collaboration & Communication:
Act as a liaison between study sponsors investigators patients and healthcare providers.
Participate in research team meetings sponsor calls and professional development sessions.
Provide education and training to new research personnel and clinical staff as needed.
This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.
Work Environment:
Evening hours may occasionally be required.
Position is primarily based on-site.
Required Qualifications
Work Experience:
4 years of experience in health sciences nursing biology or related field. Education may be substituted for experience on a year for year basis.
2 years of clinical research experience.
Experience with clinical research regulations (FDA GCP IRB HIPAA).
Preferred Qualifications
Certifications: Phlebotomy certification.
Work Experience:
4 years of clinical research experience.
Experience in pulmonary critical care or sleep medicine research.
Experience with REDCap Epic or similar data management systems.
Skills
Organization.
Problem-solving.
Communication.
Computer skills.
Comprehensive Benefits Package:
Coverage begins on day one for health dental and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance long-term disability insurance and various additional voluntary insurance plans are available. Paid time off including vacation and sick begins accruing upon hire plus ten paid holidays. One paid discretionary day is available after six months of employment and paid time off for bereavement jury duty military service and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. Type: Regular Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including but not limited to education experience and training qualifications relative to the requirements of the position and funding. At the University of Kansas Medical Center a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range taking into account the combination of factors listed above. Minimum Midpoint MaximumTime Type:
Full timeRate Type:
SalaryPay Range:
$58656.00 - $86000.00
Required Experience:
IC
Key Skills
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About Company
The University of Kansas Medical Center (KUMC), a campus of the University of Kansas located in Kansas City, Kansas, offers educational programs and clinical training through its schools of Health Professions, Medicine, Nursing, and Graduate Studies.
