Research Coordinator
Endeavor Health
Date: 1 week ago
City: Evanston, IL
Contract type: Full time
Position Highlights
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.
Diversity, equity and inclusion is at the core of who we are; being there for our patients and each other with compassion, respect and empathy. We believe that our strength resides in our differences and in connecting our best to provide community-connected healthcare for all.
EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.
- Position: Research Coordinator, DOM Resource
- Location: Evanston & Skokie, IL & locations to other sites will be required
- Full Time/Part Time: Full Time
- Hours: Monday-Friday
- Required Travel: possible travel to study start-up meetings
- Provides clinical care services including consenting, treating and monitoring of patients
- Recruit and screen candidates for clinical trials
- Acquire past medical and medication history profiles
- Ship lab samples
- Dispense research drug to patients according to protocol.
- Utilize electronic capture to update patient information.
- Helps to oversee clinical data for audits and oversight visits
- Perform a variety of research, data entry and regulatory duties of a routine and technical nature related to departmental research endeavors
- Ensure adherence to protocols and quality of information received
- Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol
- Assist with budget proposals and study budget tracking
- Assist with study time reporting
- Ensure compliance with local, state and Federal regulations for the protection of human subjects
- Complete regulatory submissions/revisions for the Institutional Review Board (IRB)
- Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion
- Complete data abstraction and data entry for study specific databases.
- Review and timely report study related adverse events to the sponsor.
- Education: Bachelor’s degree required, in the fields of social, biological or healthcare sciences preferred
- Experience: 1-5 years of research experience
- Experience with phlebotomy, ECG and pharmacy practices preferred
- Career Pathways to Promote Professional Growth and Development
- Various Medical, Dental, and Vision options
- Tuition Reimbursement
- Free Parking at designated locations
- Wellness Program Savings Plan
- Health Savings Account Options
- Retirement Options with Company Match
- Paid Time Off and Holiday Pay
- Community Involvement Opportunities
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.
Diversity, equity and inclusion is at the core of who we are; being there for our patients and each other with compassion, respect and empathy. We believe that our strength resides in our differences and in connecting our best to provide community-connected healthcare for all.
EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.
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