Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Clinical Research Coordinator 1, Rush Surgery Department

Expired Job

Rush University Medical Center Chicago , IL 60602

Posted 3 months ago

Here at Rush University Medical Center in Chicago, Illinois, we are committed to advancing scientific medical knowledge through research. We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability. Are you looking to be a part of the exciting, always evolving and expanding new developments in research here at Rush University Medical Center? Are you well experienced in working with a variety of group, single and industry oriented studies? If this describes you, you may be the right candidate for the Clinical Research Coordinator I position in the Surgery Department.

Position Highlights:The Clinical Research Coordinator I works under the general direction of the Rush Surgical Division, and in partnership with the Principal Investigator (PI), Co-Investigator(s), other study personnel, and sponsoring agents to ensure protocols are conducted in accordance with the principles of Good Clinical Practice (GCP) .S/he will coordinate clinical research studies and perform a variety of duties involved in the collection, compilation, and documentation of clinical research data. S/he plays an instrumental role in facilitating the informed consent process and ensuring compliance with the study protocol. The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.

Position Responsibilities:

  • Adheres to the policies, procedures, and guidelines instituted by Office of Research Affairs and the Office of Research Compliance.

  • Coordinates clinical research studies conducted by Principal Investigator(s) including, but not limited to grant-funded research, externally sponsored clinical research, and investigator-initiated clinical research conducted on site at Rush or its affiliated sites.

  • Works closely with the Principal Investigator to coordinate all aspects of conducting clinical trials including: screening, enrollment, and study subject visits.

  • Assists the Principal Investigator and Department/Research Administrator to review the protocol plan to develop the budget and differentiate the standard of care versus research charges while ensuring all potential costs of the trial are identified and covered by a funding source.

  • In conjunction with the Clinical Research Administration Division and Principal Investigator, determines the appropriate patient population, recruits and maintains the target number of subjects for trial participation.

  • Updates the Clinical Research Administration Division as necessary.

  • Maintains accurate and complete documentation of signed informed consent and HIPAA Authorization forms, relevant IRB approvals, source documentation, Case Report Forms (CRF's), Delegation of Authority logs , protocol training logs, and study related communication.

  • Enters data entry into the study's electronic data capture system and responses to queries in a timely manner.

  • Assists the Principal Investigator with reporting of unanticipated problems (protocol deviations, adverse events, and serious adverse events).

  • Partners with the study sponsor and Principal Investigator to complete study closure activities such as notification to study subjects, IRB, Clinical Research Administration Division, and Department/Research Administrator.

  • Communicates with study subject regarding subject procedures and visit schedule.

  • Works closely with the Clinical Research Administration Division to ensure Standard Operating Procedures (SOPs) are implemented and documented in accordance within study sponsor, Principal Investigator, and regulatory agency specifications.

  • Organizes and attends site monitoring visits conducted by internal and external auditors/monitors. May obtain, process, transport and ship potentially biohazardous specimens to appropriate laboratory according to protocol and regulatory requirements

  • Perform a variety of duties involved in the collection, compilation, and documentation of clinical research data.

  • Follow FDA, OHRP, and Rush guidelines in the collection of clinical data and/or administration of clinical studies.

  • May perform informed consent process for subject enrollment.

  • Document all study subject interactions in the subject's research records.

  • Coordinates the submission or submits documents, study protocols, and study protocol amendments to the local IRB per policy and procedure.

  • May travel offsite to study sponsor meetings.

  • Performs other duties as assigned.

Position Qualifications Include:

  • Bachelor's degree in Science/ Health Related Field is required. Post-secondary experience in Clinical Research.

  • Certification as a Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP) is preferred.

Company Highlights:

  • Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career. Everything we do centers on one goal: improving patient care.

  • Rush's 14-story medical hospital building, the Tower, is the cornerstone of the Rush campus transformation, and is the symbol of a philosophy - an evolution in the delivery of patient-centered care.

  • Rush University Medical Center is a four time Magnet facility located in Chicago, IL - www.rush.edu

  • Preeminent academic medical center, acute care hospital w/ 676 licensed beds

  • RUMC offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements.

Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Complete Application

Help

If you are experiencing technical difficulties with submitting your job application,

please send a detailed description and screenshot of the error to application_techsupport@rush.edu.

  • 2018 rush university medical center

  • Rush.edu

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Clinical Research Coordinator 1 Rush Rheumatology

Rush University Medical Center

Posted 7 days ago

VIEW JOBS 12/5/2018 12:00:00 AM 2019-03-05T00:00 Rush University Medical Center, we are committed to advancing scientific medical knowledge through research. We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability. Are you looking to be a part of the exciting, always evolving and expanding new developments in research here at Rush University Medical Center? If this describes you, you may be the right candidate for the Clinical Research Coordinator 1 position in Rush Rheumatology Position Responsibilities: * Recruits, consents, screens, schedules, tracks and provides study updates to study participants throughout the conduct of the study. * Collects and enters data into study case report forms and/or electronic data capture system and respond to queries in a timely manner. * May submit or coordinate the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure * Maintains accurate and complete procedural documentation including study participant and site level documentation in compliance with institutional, local, state and federal guidelines and regulations related to clinical research. * May collect, process and ship potentially biohazardous specimens. * Administers structured tests and questionnaires according to research study protocols. May utilize study-related technology and equipment as part of assessment procedures. * Provide ongoing study status updates and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the conduct of the study * Organize and participate in auditing and monitoring visits * Gather and communicate unanticipated problems (protocol deviations, adverse events, and serious adverse events). * Work with PI(s), sponsor, compliance, clinical staff and/or manager to identify and improve routine processes as it relates to the conduct of the research study Required Position Qualifications: * Bachelor's degree required * 2 years of research experience required * Demonstrated knowledge of Good Clinical Practices and Good Documentation Practices * Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research * Ability to meet deadlines and help coordinate multiple aspects of the ongoing project * Strong organizational and problem-solving skills * Detail oriented with high attention to accuracy * Ability to build rapport, navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants and vendors * Effective verbal and written communication skills * Ability to collaborate within multi-disciplinary team settings * Availability to work evenings, overnight and weekends if called for under the study protocols * Travel may be required Preferred Position Qualifications: * Bachelor's degree in Sciences or health-related discipline preferred * Prior participant contact experience preferred Company Highlights: * Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career. Everything we do centers on one goal: improving patient care. * Rush's 14-story hospital Tower is the cornerstone of the Rush Transformation, and is the symbol of a philosophy-an evolution in the delivery of patient-centered care. * Rush offers a competitive salary, valuable healthy living benefits to include: health, dental and vision to help you maintain and improve your health. Rush also offers several ways to invest in your future. Whether you're saving for retirement or a child's education, Rush offers benefits to help you make the most of your money…now and in the future. Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. Complete Application Help If you are experiencing technical difficulties with submitting your job application, please send a detailed description and screenshot of the error to application_techsupport@rush.edu. * © 2018 rush university medical center * Rush.edu Rush University Medical Center Chicago IL

Clinical Research Coordinator 1, Rush Surgery Department

Expired Job

Rush University Medical Center