Top 6 Crc level 1 Jobs in Chicago, Il

Clinical Research Coordinator Level 1
ICON Plc —Downers Grove, IL
- $42,600 - $53,250 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Disability insurance
- Health insurance
1d
Clinical Research Coordinator I (CRC-1)
Insight —Chicago, IL
- $50,000 - $65,000 a year
- Full-time
- Nursing
- Hospital
- Organizational skills
Quick Apply
Clinical Research Coordinator II
Loyola University Chicago —Maywood, IL
- $27 - $31 an hour
- Full-time
- Patient monitoring
- Word processing
- Computer literacy
Manager Animal Health Operations - Comparative Research Center - Full-time
Hospital: Rush University Medical Center —Chicago, IL
- $38.02 - $55.18 an hour
- 8 hour shift
- 6 years
- University
- Bachelor's degree
12d
Case Management Supervisor RN
CorVel Corporation —Downers Grove, IL
- $76,207 - $117,662 a year
- Full-time
- Nursing
- RN License
- Sales
- Health savings account
- Disability insurance
Quick Apply
Open Gym Supervisor
WILMETTE PARK DISTRICT —Wilmette, IL
- $16 an hour
- Part-time
- 18 years or older
- CPR Certification
- Mid-level
12d

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Clinical Research Coordinator Level 1

ICON Plc -
Downers Grove, IL

Apply Now

Job Details

Full-time
$42,600 - $53,250 a year
1 day ago

Benefits

Disability insurance
Health insurance
Dental insurance
Pension plan
Vision insurance
Life insurance

Qualifications

Laboratory sample storage
Vascular access
Temperature-controlled storage
Laboratory project records management
Laboratory safety
Promoting products
Hardware calibration
Adverse event reporting
Clinical incident reports
Allergy testing
Clinical skill development
Assisting with diagnostic tests and procedures
Pulmonary function testing systems
Holter monitoring
Phlebotomy specimen handling
Mid-level
Laboratory equipment calibration
Monitoring and managing IVs
Patient safety
Research project coordination
Data integrity and documentation
Clinical staff training
Records management
Bachelor's degree
Clinical data entry
Medication supplies
Clinical training
Team training
Packaging
Specimen storage protocols

Full Job Description

Clinical Research Coordinator Level 1 - Lombard, IL (Onsite)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We have an incredible opportunity for a Clinical Research Coordinator 1 to join ICON’s Accellacare team. The CRC 1 ensures the safety of our volunteers, promotes the mission of Accellacare, and strives to meet and exceed study priorities. This individual is responsible for recruiting and promoting our service to suitable participants and sponsor representatives. Additionally, the CRC 1 will perform tasks required to coordinate and complete a study according to the protocol.

This role is with Accellacare , part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

Location: 100% Onsite at Accellacare Duly Health & Care (1801 S Highland Ave, Suite 130, Lombard, IL 60148)

Hours : Monday – Friday; 8:00am – 5:00pm (no weekends or holidays)

What you will be doing:

Performing technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator
Attending investigator meetings, site initiation visits, and coordinator meetings to obtain training on drug preparation and administration and general knowledge about a protocol with a focus on clinical procedures
Obtaining knowledge about the study drugs with an emphasis on injection or intravenous infusion medications
Monitoring for possible complications with the administration of study drugs with an emphasis on injections or intravenous infusions
Maintaining accurate dispensing logs, separate from those of the coordinator, to include such information as lot number, drug vs. placebo, and information about the third-party mixer or un-blinded mixer/preparer of medication
Documenting laboratory data and adverse reactions, and immediately notifying investigators, sponsors and the Institutional Review Board, if indicated, of any unexpected or serious events
Assisting other staff members as determined by the needs and priorities of the research organization and as time and abilities permit
Actively recruiting and effectively selling our service to suitable patient participants for clinical trials with set time allotted each week for recruitment efforts
Proactively promoting the site with monitors and in-house contacts for future trials
Responding to queries in a timely manner, prompt data entry and working with the monitor during on-site visits are examples of pro-active behaviors
Preparing study documentation in the event of a sponsor or FDA audit and assisting the auditor for the duration of the audit
Ordering clinical supplies, as well as ordering, storing and monitoring of protocol specific rescue drugs and maintaining scheduled assessment of the code/crash cart and AED including maintaining proper documentation for both
Monitoring and maintaining refrigerators, freezer units and investigational product storage temperatures for safety and stability
Obtaining and maintaining knowledge in regards to temperature monitoring devices and procedures for lab specimens and investigational products and providing detailed information to all staff and sponsors in regards to how temperatures are monitored and maintained
Maintaining certification for packaging and shipping specimens on dry ice, as well as maintaining and updating knowledge of lab procedures to assist with workflow
Acting as the OSHA Representative for the site which would include but not be limited to; maintaining employee immunization records, obtaining vaccines when necessary for site or PMG and administering vaccines to staff
Performing equipment calibration when needed, if not performed by the lab coordinator or outside service and maintaining equipment calibration records
Supporting training and additional development of clinical skills for site staff as needed
May travel to other local Duly Health & Care sites within the Accellacare site network

Your Profile:

1+ years of work experience in a clinical research or pharmaceutical environment
Strong attention to detail
Motivated about a career in clinical research
Excellent time management and planning skills with an organized approach to work
Bachelor's degree in life sciences or other related field

#LI-Office

#LI-TP1

#LI-Accellacare

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Salary Range

$42,600.00-$53,250.00

Are you a current ICON Employee?

Apply Now

Refine Your Search

crc level 1 jobs in chicago, il

Clinical Research Coordinator Level 1

Clinical Research Coordinator I (CRC-1)

Clinical Research Coordinator II

Manager Animal Health Operations - Comparative Research Center - Full-time

Case Management Supervisor RN

Open Gym Supervisor

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