Clinical Research Coordinator - Cancer Center; KMCRI

Clinical Research Coordinator - Cancer Center (KMCRI)

Department: SOM KC Cancer Center Cancer Research

Job Family Group:
Professional Staff

Job Description

Summary:

The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors participants' progress—including documenting and reporting adverse events—and participates in periodic quality assurance audits of protocols.

The Clinical Research Coordinator will work with the research team led by Dr. Priyanka Sharma in breast cancer research.

• Recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials under the direction of the principal investigator.
• Maintain source documents and submit case report forms (CRFs) as required for clinical trials.
• Recognize and report adverse events and serious陪 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.
• Coordinate biological specimen collection and shipping to/from trial sites.
• Ensure adequate study supplies are 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 the Principal Investigator and Projectancode Manager as required.
• Participate in quality assurance activities by reviewing clinical data in medical chart reviews, assessing pharmacy compliance with protocol criteria, and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
• Assist in writing and formatting grant proposals, manuscripts, and study protocols.
• Assist with project planning and coordination, including identification of potential problems and recommendation of solutions or modifications.
• Work closely with the Research Institute and Human Research Protection Program and maintain a working knowledge of KUMC дуб policies and procedures.
• Attend continuing education, research and training seminars as requested by manager.

This(delil) 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 Crisis 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: This position will be 100% onsite due to the fact this is a patient‑facing role. The candidate must be located in the Kansas City metropolitan area.

• 4 years of relevant work experience. Education may be substituted for experience on a year‑for‑year basis.
• Experience with regulations governing clinical research (CFR, GCP, HIPAA).셀
• Experience with statutes and guidelines relevant to regulatory affairs in clinical research.

• Education:
  
  Bachelor's degree.
• Experience interpreting study protocols to create data management uan tracking tools.
• Experience with study budgets, contracts, and grant applications.
• Experience with electronic medical records and electronic data capture systems for clinical trials (e.g., Velos).
• Prior cancer‑related research experience (including any internship experience).

• Certified Clinical Research Coordinator (CCRC)
• Certified Clinical Research Professional (CCRP)

• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Ability to learn new software and systems.
• Organizational, problem‑solving, and interpersonal skills.
• Communication.
• Multitasking.

• Resume
• Cover Letter

Coverage begins on day one for health, dental, and…