Clinical Research Associate Jobs in Illinois
ICON Clinical Research Multiple
Home Based Clinical Research Associate Travel up to 80% ( Sites throughout the country) Phase I-IV experience desired Candidate can be based anywhere in the USA Perform assessment site visits to assure study implementation and monitoring activities are conducted according to expectations (as described in the monitoring plan ) The monitor adequately prepares for the Monitoring visit by reviewing si...
Judge Healthcare is actively seeking a CRA( Clinical Research Associate) for a leading Bio Pharma client in the Lake Forest, IL area. This is a project assignment slated to run from early January 2014 to early April 2014. PRIMARY FUNCTION: Supports and assists Clinical Project Managers (CPM) and the Clinical Operations team with execution of clinical research studies to develop safe and efficaciou...
Job Title: Clinical Research Associate Position Responsibilities Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and traini...
EDUCATIONAL BACKGROUND: Bachelors Degree (Science or Health Related Field is Preferred) Certified Clinical Research Associate required EXPERIENCE: Minimum of 3-5 year experience working as Clinical Research Associate (CRA), 1 year as a Sr. CRA Previous Pharma industry experience is required • Previous experience functioning as an unblinded Clinical Research Associate is preferred • Previous experi...
Good Day, We have an urgent opening for the profile of Clinical Research Associate with one of our clients located in North Chicago, IL 60064. Please find the job description mentioned below: if you feel interested you can email me your resume at ***** or you can call me at 919 887 6786 X4083 Job Title: Clinical Research Associate Location: North Chicago, IL 60064 Duration: 6+ m...
6 Month Contract Position:: · This is an in-house CRA. · TA is Antiviral, specifically HCV. · Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. · Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and m...
6 Month Contract Position: · Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. · Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning...
The Regional CRA performs activities associated with the site-level feasibility, evaluation, initiation, patient recruitment and retention, monitoring and collection of data, and closeout of clinical trial sites in the geographic area assigned to them. Regional CRA Job Responsibilities: · Completes site-level feasibility tools/questionnaires · Develops monitoring plan · Conducts clinical site visi...
Good Day, We have an urgent requirement for Clinical Project Managerat North Chicago IL 60064 with one of our clients. Please go through the job description and if you will find it interesting then send me an updated copy of your resume. Position: Clinical Project Manager Location: North Chicago IL 60064 Duration: 6+ months Description: · Experience with Clinical Contract Negotiation and budgeting...
PS Order #: 0000092278 Title of Position: Associate Director Exploratory Statistics Location: Chicago, IL REQUIRED Qualifications: PhD in Statistics, Biostatistics, computational direct line management experience minimum 2 years, demonstrated mentoring ability, experience in discovery, clinical biomarker (genomics, genetics, imaging), pre-clinical DESIRED Qualifications: PhD in Statistics or Biost...
This position can be home-based from the following states: Texas, Oklahoma, Kansas, Missouri, Nebraska, Iowa, Indiana, Illinois, Michigan, Wisconsin, North Dakota or South Dakota. The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and...
Company Information Thermo Fisher Scientific is the world leader in serving science. The company enables its customers to make the world healthier, cleaner and safer by providing analytical instruments, equipment, reagents and consumables, software and services for research, analysis, discovery and diagnostics. With annual sales of $13 billion, Thermo Fisher Scientific has over 39,000 employees an...
Company Information About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of more than $10 billion, we have approximately 35,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic la...
Posting date: November 19, 2013 Company Information About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of more than $10 billion, we have approximately 35,000 employees and serve customers within pharmaceutical and biotech companies, hosp...
Summary: The Sr. Medical Education Specialist will act as central point of contact for clinical site coordinator and Primary Investigator of investigator initiated studies. Assures all required documentation is received (study protocols, medical license, IRB approval, signed contracts, etc), reviews documents for consistency with Hospira and regulatory requirements; maintains and archives internal...
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Answers for Clinical Research Associate Jobs
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How soon before graduation should I start applying for jobs?
I'm graduating in May with a Bachelor's degree in Political Science, and I'm looking into jobs as a Clinical Research Coordinator/Associate. How soon before graduation should I start applying for jobs...
How does one become a Clinical Research Associate?
I recently graduated with a PhD in Life Sciences and want to become a CRA. How should I go about this process? There are several online courses being offered that promise job assistance. Would they re...
How much salary a clinical research associate gets in Maryland with 1 year of relevant experience.Th...
It is a Pharmaceutical company with branches in 40 countries and 2,000 employees. In my current job I do everything a CRA does except traveling. So I make a very good CRA. Also could some one pleas...
How can a pharmaceutical manufacturing team leader get into a Clinical Research Associate role?
I am a Biology graduate that has worked in Clinical manufacturing and want to move into the Clinical Trials field, jobs are hard to get right now but how can I get into this area? Any help much apprec...
What are your chances of getting a job as a CRA?
If you take up some online program for Clinical Research Associate, does this significantly improve your chances of getting a job as a CRA? how about if you live in the philippines, can you get a job ...
Healthcare Career Tools
Clinical Research Associate
$32,900.00 - $95,000.00
Typical Salary for Clinical Research Associate in Illinois
Source: Monster.com Careerbenchmarking Tool
Education / Training
Source: Monster.com Careerbenchmarking Tool
Clinical Research Associate
Supports clinical trials by planning, collecting, screening, and summarizing information gathered.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Authors/CoAuthors study protocols, develops study documents, identifies and enlists clinical sites, ensures availability of all clinical trial materials, facilitates IRB approval, trains investigators and their staff on the study procedures, oversees and monitors trials, maintains contact information, manages data and query resolution, ensures appropriate data analysis and writes the final report.
Protects organization's value by keeping research information confidential.
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