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Clinical Research Coordinator III

Ann & Robert H. Lurie Children’s Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children’s Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report.

Location

American Dental Associates (ADA)

Job Description

Coordinates all clinical research activities with minimal supervision. Adheres to the service values and principles as well as the principles of research ethics. Based on specific research program needs, patient facing vs. data administrative responsibilities will vary. 

Essential Job Functions:

  • Coordinates and oversees all aspects of clinical research projects, including study start-up, site qualifications, initiation, monitoring, and close-out visits.

  • Oversees site visits, promptly addresses sponsor queries, and ensures strict adherence to study protocols and regulatory requirements throughout all study activities.

  • Manages regulatory compliance and documentation processes, including preparing and maintaining regulatory documents, registering studies on clinicaltrials.gov if required, assisting investigators with regulatory submissions such as to the FDA, and developing and updating Standard Operating Procedures (SOPs) to ensure adherence to research protocols and regulatory standards.

  • Promotes ethical conduct in research and ensures integrity in all aspects of study conduct and data handling. 

  • Manages logistical and administrative aspects of clinical research projects by maintaining inventory of supplies and equipment, preparing lab kits and requisitions, organizing, and maintaining study documents including regulatory binders and source documents, tracking deadlines for grants and deliverables, and constructing codebooks for data dictionaries.

  • Manages participant engagement throughout clinical research studies by identifying and recruiting eligible subjects, conducting informed consent/assent processes, coordinating subject reimbursement, verifying participant eligibility, and serving as the primary point of contact for study-related inquiries and support.

  • Manages the data lifecycle in clinical research by abstracting information from medical records, entering data into case report and study forms, preparing abstracted/coded data for analysis, conducting statistical analyses, and ensuring database validity and integrity through QA/QC checks and data monitoring processes.

  • Manages some financial aspects of research projects by assisting in budget preparation and fund review, as well as supports the research central offices and Principal Investigator (PI) in grant preparation and reporting activities.

  • Provides comprehensive training and mentorship to research personnel by assisting in study conduct training, serving as a mentor and resource, and assists the onboarding process for new study team members.

  • Leads the dissemination of research findings through manuscript preparation, collaboration on abstracts/posters, presentation of research at national meetings, or coordination of research education conferences.

  • Other job functions as assigned.

Knowledge, Skills, and Abilities:

  • Bachelor’s degree and two or more years research experience required.  

  • Two-three years with complex research projects preferred.

  • Strong organizational skills with ability to manage multiple simultaneous studies. 

  • Strong verbal and written communications skills. 

  • Strong knowledge of FDA, HSR, and GCP Guidelines. 

  • Strong analytical skills with the ability to recognize quantitative and qualitative research methods and remain agile and adaptable to various technological systems. 

  • May assist in technology system implementation.

  • Strong leadership skills with the ability to prioritize tasks, problem solve, and serve as a mentor. Ability to foster an inclusive environment where all team members feel valued and respected. 

Education

Bachelor's Degree (Required)

Pay Range

$59,280.00-$96,928.00 Salary

At Lurie Children’s, we are committed to competitive and fair compensation aligned with market rates and internal equity, reflecting individual contributions, experience, and expertise. The pay range for this job indicates minimum and maximum targets for the position. Ranges are regularly reviewed to stay aligned with market conditions. In addition to base salary, Lurie Children’s offer a comprehensive rewards package that may include differentials for some hourly employees, leadership incentives for select roles, health and retirement benefits, and wellbeing programs. For more details on other compensation, consult your recruiter or click the following link to learn more about our benefits.

Benefit Statement

For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:

Medical, dental and vision insurance

Employer paid group term life and disability

Employer contribution toward Health Savings Account

Flexible Spending Accounts

Paid Time Off (PTO), Paid Holidays and Paid Parental Leave

403(b) with a 5% employer match

Various voluntary benefits:

  • Supplemental Life, AD&D and Disability

  • Critical Illness, Accident and Hospital Indemnity coverage

  • Tuition assistance

  • Student loan servicing and support

  • Adoption benefits

  • Backup Childcare and Eldercare

  • Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members

  • Discount on services at Lurie Children’s facilities

  • Discount purchasing program

There’s a Place for You with Us

At Lurie Children’s we embrace and celebrate diversity and equity in a serious way. We are committed to building a team with a variety of backgrounds, skills, and viewpoints — recognizing that diverse identities strengthen our workplace and the care we can provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging and allyship. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care.  

Lurie Children’s and its affiliates are equal employment opportunity employers.  We value diversity and are committed to creating an inclusive environment for all employees.  All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.

Support email: candidatesupport@luriechildrens.org

Average salary estimate

$78104 / YEARLY (est.)
min
max
$59280K
$96928K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Clinical Research Coordinator III, Lurie Children's

Join Ann & Robert H. Lurie Children’s Hospital of Chicago as a Clinical Research Coordinator III and play a pivotal role in advancing pediatric care through cutting-edge research. In this dynamic position, you'll coordinate all clinical research activities with a focus on enhancing the lives of children and their families. You'll manage various aspects of studies, from start-up to close-out, ensuring strict adherence to protocols and regulatory requirements. Your strong organizational skills will shine as you oversee participant engagement, liaise with research teams, and maintain all study documentation. At Lurie Children’s, you'll take pride in promoting ethical research conduct and integrity in data handling. With a dedicated commitment to mentorship, you'll train and guide fellow research personnel while contributing to the dissemination of significant research findings at national conferences. Located in the heart of Streeterville, Chicago, our hospital is recognized for its exceptional care and innovative approach to pediatric health. Here, your contributions will truly make a difference, adding value to our long-standing legacy of excellence in patient care. Come and be a vital part of our mission to provide the best outcomes for the children we serve, all while enjoying a collaborative and inclusive work environment.

Frequently Asked Questions (FAQs) for Clinical Research Coordinator III Role at Lurie Children's
What responsibilities does a Clinical Research Coordinator III at Ann & Robert H. Lurie Children’s Hospital of Chicago have?

As a Clinical Research Coordinator III at Ann & Robert H. Lurie Children’s Hospital of Chicago, you will oversee all aspects of clinical research projects, including study initiation, monitoring, and compliance with regulatory requirements. You will manage participant engagement, coordinate logistics, and ensure that ethical standards are maintained throughout the research process.

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What qualifications do I need to apply for the Clinical Research Coordinator III position at Ann & Robert H. Lurie Children’s Hospital of Chicago?

To apply for the Clinical Research Coordinator III position at Ann & Robert H. Lurie Children’s Hospital of Chicago, candidates must possess a Bachelor's degree and a minimum of two years of research experience. Experience with complex projects is preferred, along with strong organizational, analytical, and communication skills.

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What skills are essential for a successful Clinical Research Coordinator III at Ann & Robert H. Lurie Children’s Hospital of Chicago?

Success as a Clinical Research Coordinator III at Ann & Robert H. Lurie Children’s Hospital of Chicago requires strong organizational skills, the ability to manage multiple studies, proficiency in FDA and GCP guidelines, and excellent analytical skills. Leadership and effective mentorship abilities are also crucial for fostering a supportive environment.

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How does Ann & Robert H. Lurie Children’s Hospital of Chicago support diversity and inclusion for Clinical Research Coordinator III roles?

Ann & Robert H. Lurie Children’s Hospital of Chicago values diversity and inclusion as integral components of its mission. As a Clinical Research Coordinator III, you will work in an environment that celebrates diversity, where different backgrounds and perspectives are recognized as strengths in providing care and enhancing workplace culture.

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What kind of benefits can a Clinical Research Coordinator III expect at Ann & Robert H. Lurie Children’s Hospital of Chicago?

A Clinical Research Coordinator III at Ann & Robert H. Lurie Children’s Hospital of Chicago can expect a comprehensive benefits package that includes medical, dental, and vision insurance, paid time off, retirement savings plans, and various wellness programs. The hospital is committed to ensuring that employees feel valued and supported.

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Common Interview Questions for Clinical Research Coordinator III
How do you manage compliance with research protocols as a Clinical Research Coordinator III?

In managing compliance with research protocols, I ensure that study activities align with regulatory guidelines and institutional policies. I regularly review protocols and documents, conduct training for team members, and actively monitor data integrity, promoting an ethos of ethical conduct in all research efforts.

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Can you describe your experience with participant engagement in clinical research?

My experience with participant engagement involves actively recruiting and communicating with study subjects, conducting informed consent processes, and serving as the primary point of contact. I prioritize building trust with participants to ensure their comfort and commitment throughout the research study.

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What strategies do you use to maintain organization in managing multiple studies?

To maintain organization while managing multiple studies, I utilize project management tools to track deadlines and deliverables. I create structured timelines for each project, maintain meticulous documentation, and prioritize tasks based on urgency and complexity, ensuring that no detail is overlooked.

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How do you handle queries from study sponsors?

When handling queries from study sponsors, I respond promptly and comprehensively, addressing their concerns based on the specifics of the study protocols. Effective communication and thorough understanding of the project details are key to maintaining a positive relationship with sponsors.

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What role do you see data integrity playing in clinical research?

Data integrity is paramount in clinical research as it ensures that the findings are credible and reliable. I implement processes for quality assurance and quality control during data collection and entry, routinely checking for accuracy and consistency to uphold the integrity of research outcomes.

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How do you promote ethical conduct within your research team?

I promote ethical conduct by fostering an environment that values transparency and accountability. I communicate the importance of ethical standards, provide training on research ethics, and lead by example in adhering to best practices and regulatory requirements.

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Describe how you approach mentorship with junior staff in the research team.

My approach to mentorship involves offering guidance and support through hands-on training and sharing my experience. I create an open-door policy where junior staff can seek advice freely and ensure they feel valued as part of the team, promoting their professional growth.

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What kind of statistical analyses have you conducted in your previous research roles?

In my previous research roles, I have conducted various statistical analyses, such as regression analyses, ANOVA, and descriptive statistics. I utilize software like SPSS and R to analyze data sets, interpret results, and ensure that findings align with research objectives.

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How do you keep up with changes in FDA guidelines impacting clinical research?

To stay updated on changes in FDA guidelines, I follow relevant publications, participate in professional associations, and attend workshops and conferences. This proactive approach helps me to adapt to new regulations and implement necessary changes in research protocols.

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What motivates you to work in pediatric clinical research?

I am particularly motivated to work in pediatric clinical research because of the profound impact our work has on children and their families. Contributing to research that improves pediatric care resonates deeply with my personal and professional values, fueling my passion for this field.

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DATE POSTED
April 4, 2025

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