Clinical Research Coordinator 2 Job at The University Of Chicago, Chicago, IL

WGlNSHR1bTY5b09mVWxkYVJuR2F5SUZ1NkE9PQ==
  • The University Of Chicago
  • Chicago, IL

Job Description

Clinical Research Coordinator 2 Clinical Research Coordinator 2 Apply remote type Hybrid locations Chicago, IL time type Full time posted on Posted 3 Days Ago job requisition id JR28795 Department BSD PED - Clinical Trials Office: COG and HemOnc Research About the Department In the Department of Pediatrics at the University of Chicago, we strive to provide the highest level of complex care for children from diagnosis and treatment to conducting research to find promising new therapies with a focus on teaching. We are committed to advancing the frontiers of knowledge, and the education and training of future clinical pediatricians, subspecialists, educators, clinical investigators and physician-scientists. The Pediatric Clinical Trials Office (Peds CTO) provides services and high-level guidance to individuals involved in human subjects research. Job Summary The Clinical Research Coordinator 2 (CRC2) provides support to the Section of Pediatric Hematology and Oncology. The CRC2 will be involved in multiple research trials types: investigator-initiated, multi-centered cooperative group studies, multi-institutional pharmaceutical trials, and multi-centered trials. The CRC2 supports, facilitates, and coordinates independently the daily clinical research activities. Our department follows a hybrid work structure that fosters productivity, collaboration, and employee well-being. Working from the office is encouraged for tasks that require a high degree of collaboration. Responsibilities Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management. Prepares program conference lists for multidisciplinary conferences and workshops. Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study. Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports. Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques. Coordinate the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence. Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures. Protect patients and data confidentiality by ensuring security of research data and personal health information. Ensures Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications. Maintains accurate and complete records which may include signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), and study related communication. Ensures compliance with federal regulations and institutional policies. May assist in the training of new or backup coordinators. Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. Performs other related work as needed. Minimum Qualifications Education: Minimum requirements include a college or university degree in related field. Work Experience: Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline. Preferred Qualifications Education: Bachelor’s degree. Experience: 2 years of clinical research experience coordinating multiple and variety of studies. Working Conditions Eligible for hybrid work based on business needs and the demands of specific tasks. Application Documents Resume (required) Cover Letter (required) The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans employer. All offers of employment are contingent upon a background check that includes a review of conviction history. The University of Chicago's Annual Security & Fire Safety Report provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online #J-18808-Ljbffr The University Of Chicago

Job Tags

Full time, Work experience placement,

Similar Jobs

Jobot

2nd Shift Production Supervisor (Hiring Immediately) Job at Jobot

 ...offering various salad choices, snacks, and meal kits. Job Details Job Details: We are looking for a dynamic and experienced 1st Shift Production Supervisor to join our manufacturing team. This is a full-time, permanent position on the 1st shift. The successful... 

Glenda Culbertson

Pay Per Click (PPC) Manager Job at Glenda Culbertson

We are seeking a PPC (Pay Per Click) Manager to plan and run our PPC campaigns. You will be also required to track and manage our paid search budgets.As a PPC (Pay Per Click) Manager, you will be responsible to do search engine marketing (SEM) including search engine... 

Clinical Staffing Resources New York

Direct Support Specialist ( DSP) Job at Clinical Staffing Resources New York

 ...Job Description Job description DSP (Direct Support Professional) Sunshine Care Network Join our Team of Sunshine Care Network Providers! We believe that no parent or child should stand alone. Instead, parents and families are enhanced by our Caring team of... 

Patterns Behavioral Services, Inc.

Board Certified Behavior Analyst (BCBA) - Orange County, CA Job at Patterns Behavioral Services, Inc.

 ...you will find a professional, ethical, structured, respectful, caring, and fun work environment where you can reach your career goals!...  ...sound decision-making skills Full-Time, Non-Exempt The health and safety of our employees and of those individuals we serve is... 

DocStar Medical Partners

Pediatric - Adolescent Medicine Physician Assistant Job at DocStar Medical Partners

Docstar is working with a client of ours that is looking for a Pediatric Physician Assistant for a Locum Tenens position in Stockinton, CA. Expenses are covered if not local to Stockton. Start Date: Asap or 2 weeks from interview Length of Assignment: 3 months...