Hourly Pay Range:

Position Highlights:

• Position: Clinical Research Associate- Pediatrics /Family Medicine
• Location: Evanston, IL
• Full Time
• Hours: Monday-Friday, [hours and flexible work schedules]
• Required Travel: Candidate must be willing to travel

A Brief Overview:
Endeavor Health’s department of Pediatrics and department of Family Medicine is seeking applicants for Clinical Research Associate (CRA). Primary responsibility for this position is the management and oversight of several research projects (possibly involving multiple data collection sites) involving human subjects, particularly medical patients. The CRA provides support to the Research Manager, CRU director, Physicians, and Research Scientists in the Departments of Pediatrics and Family Medicine. The CRA assists in consenting of patients to research studies, IRB processing and compliance with federal, state, local, and institutional research regulations, writing grants for submission to external funding agencies. Manages all aspects of interactions with the Endeavor Health IRB for designated/assigned projects. This position is responsible for administering the processes and procedures necessary to ensure compliance with the requirements of the Endeavor Health IRB and external funding agencies such as budget management, progress reports, and protocol revisions. The duties of this position are typically performed in coordination with study investigators to plan and implement new research projects, assistance with design of data collection and tracking forms, development and implementation of data tracking procedures, coordination and liaison with other research sites, training and oversight of data collection personnel, monitoring quality assurance for data collection, management of study databases with assistance from programmers and statisticians, and production of data reports for tracking purposes. This position will involve subject recruitment, data collection, and the performance of other research project-related tasks, as needed.

What you will do:

• Ensure compliance with applicable federal, state, local, IRB, and Good Clinical Practice (GCP) regulations.
• Support all aspects of human-subject clinical research across Pediatrics and Family Medicine.
• Collaborate with Research Managers, Principal Investigators (PIs), Research Scientists, sponsors, and national/international collaborators.
• Evaluate the feasibility, resources, timelines, and financial requirements of proposed studies.
• Develop, adapt, and maintain research protocols, consent forms, study documents, and regulatory materials.
• Prepare and submit IRB applications, amendments, renewals, adverse events, progress reports, and responses.
• Ensure research staff maintain required human-subject training and certifications.
• Recruit, screen, enroll, and consent study participants; determine eligibility and perform randomization as required.
• Coordinate and assist with study visits, patient care, scheduling, and protocol procedures.
• Maintain communication with participants and provide education and resources to support protocol compliance.
• Coordinate specimen collection, processing, storage, and shipment, including blood, urine, and tissue samples.
• Retrieve, collect, enter, and maintain research data and subject records; ensure accuracy and completeness of case report forms and source documents.
• Manage study files, databases, supplies, payments, equipment, test articles, and document retention.
• Monitor study progress, expenditures, accounts, timelines, adverse events, and protocol compliance.
• Prepare for and support monitoring visits, audits, and study closeout activities.
• Assist with research study design, database development, data collection strategies, and analysis.
• Conduct literature reviews and support preparation of protocols, manuscripts, abstracts, presentations, posters, and publications.
• Coordinate and support grant submissions, including budgets, CVs, biosketches, supporting documents, and funding opportunities.
• Develop and maintain research databases, websites, procedure manuals, and study-related resources.
• Create study advertisements and communications in collaboration with marketing/public relations.
• Participate in research meetings, conferences, and departmental initiatives.
• Provide supervision, training, and orientation to research staff as needed.
• Perform other research-related duties and projects as assigned by the Research Manager.

What you will need:

• Education: Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree in a major such as biology, social, or health science or related
• Experience:: Minimum 2 years' experience as a research coordinator in clinical trials research (or equivalent position) required, experience with drug and or device research preferred.
• Experience; Facilitating recruitment and follow up strategies with clinic personnel and operational problem solving
• Proficient knowledge of FDA, HSR, and GCP guidelines
• Excellent organization, time management, problem solving and communication (both written and verbal) skills
• Ability to interact in a professional and sensitive manner with medical personnel, research subjects, research collaborators, community groups and other research staff
• Must be able to work independently or with minimal supervision, and show initiative
• Experience with EPIC and Workday preferred

Benefits (For full time or part time positions):

• Eligibility for our Annual Incentive Plan, which offers the potential to earn a certain percentage amount of your base salary based on organizational performance. (For AIP eligible positions)
• Premium pay such as shift, on call, holiday and more based on an employee’s job (For eligible positions)
• Incentive pay for select positions
• Opportunity for annual increases based on performance
• Career Pathways to Promote Professional Growth and Development
• Various Medical, Dental, Pet and Vision options
• Tuition Reimbursement
• Free Parking
• Wellness Program Savings Plan
• Health Savings Account Options
• Retirement Options with Company Match
• Paid Time Off and Holiday Pay
• Community Involvement Opportunities

Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties. Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. For more information, visit www.endeavorhealth.org.  

When you work for Endeavor Health, you will be part of an organization that encourages its employees to achieve career goals and maximize their professional potential.

Please explore our website (www.endeavorhealth.org) to better understand how Endeavor Health delivers on its mission to “help everyone in our communities be their best”. 

Endeavor Health is committed to working with and providing reasonable accommodation to individuals with disabilities. Please refer to the main career page for more information.

At Endeavor Health, we are united by a shared commitment to working together to create a culture of connection and belonging—each of us bringing different skills and experiences as we deliver safe, seamless, and personal care. Every person, every time. We are committed to fostering an environment where all team members can be their best, learn, and pursue excellence together.

EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.