Clinical Research Coordinator Associate
- Downers Grove
- ICON Full Service & Corporate Support
- Clinical Research Site Services
- Office Based
TA Business Partner
- Full Service Division
About the role
CRC Associate-Downer's Grove, IL-Office Non Flex
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Title: CRC Associate
Location: Onsite - Oak Lawn, IL/Tinley Park
Responsibilities:
- Assisting Clinical Research Coordinators with patient visits, documentation, CRF completion, data queries and monitor visits
- Performing technical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator
- Assisting in the laboratory or with other laboratory duties such as performing quality assurance review, restocking of supplies and processing of specimens
- Performing consult visits as needed
- Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment
- Assisting the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures
- Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
- Addresses all queries or data clarifications within 48 hours of receipt
- Typing memos, letters, recruitment tools, progress notes and various documents
- Filing labs and correspondence
- Performing various errands to pick up dry ice, supplies, samples, physician signatures and storage boxes, etc
- Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit
- Assisting with answering the telephones, making appointment reminder calls and initial phone screening
- Travel: Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed
Qualifications:
- Minimum of a Bachelor's degree Life Sciences, Healthcare, or related field
- 1-2 years of Clinical Research or related experience
- Ability to multi-task and support multiple projects/studies
- Experience in MS Office Suite
#LI-SB4
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
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