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Crc Global Jobs (NOW HIRING)

ICON

CRC Level 1

Lombard, IL · On-site

$23.75 - $31.75/hr

The CRC 1 ensures the safety of our volunteers, promotes the mission of Accellacare, and strives to ... Our global site network is designed with one goal in mind: to deliver better access, greater ...

CRC Group

Tax Senior Manager

Charlotte, NC · On-site

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CRC Group

Tax Senior Manager

Charlotte, NC · On-site

$140 - $195/hr

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... CRC Group is a Drug Free Workplace.*** #J-18808-Ljbffr

New

CRC Group

$140 - $195/hr

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... CRC Group is a Drug Free Workplace.*** #J-18808-Ljbffr

New

Revolution Medicines

Director, Global Marketing

The Directors of Global Marketing will support the pancreatic, lung, and/or CRC cancer teams and will help shape and enable Revolution Medicines' global go-to-market and launch plans across key ...

Revolution Medicines

Director, Global Marketing

The Directors of Global Marketing will support the pancreatic, lung, and/or CRC cancer teams and will help shape and enable Revolution Medicines' global go-to-market and launch plans across key ...

Syneoshealth

CRC II (Onsite) - Marietta, GA

Concord, NC · On-site

$22.50 - $30/hr

CRC II (Onsite) - Marietta, GA Illingworth Research Group provides a range of patient focused ... Illingworth Research Group is a global organization operating in over 45 countries, bringing ...

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

CRC II (Onsite) - Marietta, GA Illingworth Research Group provides a range of patient focused ... Illingworth Research Group is a global organization operating in over 45 countries, bringing ...

Google

Global Accommodations Lead, Benefits

Boulder, CO · On-site

$16 - $22/hr

Master's degree, Juris Doctor (JD), or professional certification (e.g., SPHR, CRC, CDMS). * 7 ... About the job The Global Benefits and Mobility team supports Googlers and their loved ones during ...

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Crc Global information

What are some common challenges faced by professionals working at CRC Global, and how can new employees prepare for them?

At CRC Global, professionals often operate in fast-paced, collaborative environments where they must manage multiple projects and clients simultaneously. New employees may find it challenging to quickly adapt to evolving client needs and maintain effective communication across cross-functional teams. To succeed, it's helpful to develop strong organizational skills, stay proactive in seeking feedback, and be open to learning from experienced colleagues. Embracing the company's culture of teamwork and continuous improvement can also help new hires navigate these challenges successfully.

What are the key skills and qualifications needed to thrive as a CRC (Clinical Research Coordinator), and why are they important?

To thrive as a Clinical Research Coordinator, you need a solid background in clinical research, medical terminology, and regulatory compliance, often supported by a degree in a health-related field and certifications like CCRC or CCRP. Familiarity with electronic data capture systems, clinical trial management software, and Good Clinical Practice (GCP) guidelines is essential. Excellent organizational skills, attention to detail, and strong interpersonal communication help you manage studies and interact with participants and research teams. These competencies ensure that clinical trials are conducted ethically, accurately, and efficiently, safeguarding participant safety and research integrity.

What is the difference between Crc Global vs Crc Technician?

AspectCrc GlobalCrc Technician
CertificationsTypically requires industry-specific certifications, such as CRC certification or related credentialsRequires similar certifications, often including CRC certification and technical training
Work EnvironmentOften involves project management, client interaction, and overseeing multiple sitesPrimarily hands-on technical work at specific sites or facilities
Employer & Industry UsageUsed by companies providing comprehensive CRC services, including consulting and project managementCommonly employed by service providers performing technical CRC tasks

The main difference is that Crc Global typically refers to a broader, managerial, or consulting role overseeing CRC projects, while Crc Technician focuses on technical, hands-on tasks. Both roles require similar certifications, but their responsibilities and work environments differ significantly.

What is a CRC Global?

A CRC Global typically refers to a Clinical Research Coordinator (CRC) who works on global or international clinical trials. This role involves managing and overseeing clinical studies across multiple countries, ensuring compliance with international regulations, and coordinating with diverse research teams. CRC Globals are responsible for patient recruitment, data collection, and maintaining study documentation while navigating the challenges of cross-cultural communication and varying regulatory requirements. Their work is essential for the success of global pharmaceutical and medical research projects.

What cities are hiring for Crc Global jobs?

Cities with the most Crc Global job openings:

What states have the most Crc Global jobs?

States with the most job openings for Crc Global jobs include:

What job categories do people searching Crc Global jobs look for?

The top searched job categories for Crc Global jobs are:

Crc Global jobs near you
Infographic showing various Crc Global job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution.

CRC Level 1

ICON

Lombard, IL • On-site

$23.75 - $31.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago

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 here.
Salary Range
$42,600.00-$53,250.00
Are you a current ICON Employee? Please click here to apply

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