Clinical research specialist Jobs in Peoria, IL
Last updated: 14 hours ago
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward.As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by ...Show moreLast updated: 13 days ago
When our values align, there's no limit to what we can achieve.The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active par...Show moreLast updated: 15 days ago
At SSM Health, we believe in providing our employees with a fulfilling career.We strive to create an environment where individuals can grow both personally and professionally.Our company values div...Show moreLast updated: 30+ days ago
The Agricultural Research Service (ARS) is the United States Department of Agriculture's chief scientific research agency and one of the world's premiere scientific organizations.ARS Postdoctoral R...Show moreLast updated: 2 days ago
BSD MED - Infectious Diseases - Chicago Center HIV Elimination - Implementation Research.This role will be housed in central Illinois, specifically Springfield, IL to support projects off campus in...Show moreLast updated: 30+ days ago
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.When considering candidates, we look for scientific and business professionals wh...Show moreLast updated: 30+ days ago
At Genworth, we empower families to navigate the aging journey with confidence.We are compassionate, experienced allies for those navigating care with guidance, products, and services that meet fam...Show moreLast updated: 30+ days ago
The Clinical Documentation & Coding Specialist (CDCS) plays a critical role in ensuring accurate and comprehensive documentation within Alteas Health’s clinical and administrative systems.This pos...Show moreLast updated: 18 hours ago
We provide our employees with a generous benefits package including : .Competitive salary - PLUS time and a half paid for hours worked over 40 per week.
Company paid holidays, PLUS 1 floating holiday...Show moreLast updated: 14 hours ago
BD is one of the largest global medical technology companies in the world.Advancing the world of health™ is our Purpose, and it’s no small feat.
It takes the imagination and passion of all of us—fro...Show moreLast updated: 30+ days ago
Sound Physicians is a leading hospitalist company that delivers improved quality of inpatient hospital care, the highest levels of patient and physician satisfaction ratings and exceptional operati...Show moreLast updated: 30+ days ago
Overview Expected pay for this position is $32.Actual pay will be determined by experience, skills and internal equity.POSITION SUMMARY : The Clinical Research Billing (CRB) Analyst plays a crucial ...Show moreLast updated: 30+ days ago
Clinical Research Associate
PRA Health SciencesIL, US As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Contribute to the identification of new sites for clinical t...Show moreLast updated: 30+ days ago
Senior Clinical Research Associate - CNS - Midwest
Worldwide Clinical TrialsIllinois, USA Senior Clinical Research Associate.Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies...Show moreLast updated: 30+ days ago
Clinical Implementation Specialist
Zimmer BiometIllinois, Illinois, United States$70,000.00–$85,000.00 yearly
(Sr.) Clinical Research Associate - Midwest - FSP
ParexelRemote, Illinois, United StatesRemote
Full-time
RN - Clinical Documentation Specialist
SSM HealthREMOTE, IL, USRemote
Full-time
- Promoted
Research Plant Pathologist / Plant Physiologist / Geneticist (Research Associate)
Agricultural Research ServicePeoria, IL, United StatesFull-time +1
Research Specialist
University of ChicagoIllinoisPart-time
Senior Clinical Research Associate - Central / Midwest
BeiGeneUS, IL, Home$97,100.00–$132,100.00 yearly
Remote
Full-time
RN- Clinical Admission Specialist
CarlePeoria, IL RN- Clinical Admission Specialist.Department : Transfer Coordination - CMH.Experience Required : 3 - 5 Years.Education Required : Associates Degree.
Work Location : Working from Home.Show moreLast updated: 30+ days ago
Claims Clinical Specialist – Medical Review Team
Genworth FinancialIllinois$124,600.00 yearly
Remote
Full-time
- New!
Clinical Documentation & Coding Specialist
Alteas HealthRemote, IL, United States$65,000.00–$85,000.00 yearly
Remote
Full-time
Quick Apply
- Promoted
- New!
CLINICAL TECHNOLOGY SPECIALIST
ForTec MedicalIL, United States$40,000.00–$50,000.00 yearly
Full-time
Clinical Specialist - RN (Chicagoland)
BDIllinois,USAFull-time
Clinical Support Specialist - Remote - Contract
Sound PhysiciansIL, IL , USRemote
Full-time
Clinical Research Billing Analyst
OSF HealthcarePeoria, Illinois, US$32.87–$38.66 hourly
Research Specialist (Cancer Biology and Pharmacology)
University of Illinois ChicagoPeoria, IL, US Research Specialist (Cancer Biology and Pharmacology).The Department of Cancer Biology and Pharmacology at the University ofIllinois College of Medicine Peoria (UICOMP) seeks a talented professiona...Show moreLast updated: 30+ days ago
- Promoted
Senior Research Administrator
Beacon Hill Staffing Group, LLCDouglas, Illinois, United States Y2hpYXQuODgxMTMuNDc5QGJlYWNvbmhpbGwuYXBsaXRyYWsuY29t.Beacon Hill has partnered with a reputable university in hiring a Senior Research Administrator to start immediately.
This is a contract role for...Show moreLast updated: 8 days ago
Clinical Research Associate
PRA Health SciencesIL, US30+ days ago
Job descriptionImplement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes. Identify problems at sites; resolve issues and escalate as appropriate. Collaborate with the CSM to ensure recruitment and execute contingency plans, as needed. Complete preparation and generation of visit monitoring reports as per relevant SOP Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets. If working with central CRAs (blinded and un-blinded), respond to alerts and follow-up to ensure resolution of issues Implement site close-out activities and generate site close-out report. Provide feedback on site performance for future trial site feasibility / selection Improve skills by timely completion performance of assigned global and local training. Minimum 18 months prior monitoring experience with global trials.In-depth knowledge of FDA regulations and ICH / GCP guidelines Bachelors of Science Excellent interpersonal and communication skills (verbal & written), including proficiency in medical terminology and computer systems Ability to work effectively with investigators and other research personnel, maintaining a professional demeanor Ability to independently resolve site or study related issues Self motivated; detail oriented; team player; flexible Ability to prioritize workload to meet project timelines, while managing multiple protocols across therapeutic areas Excellent organizational and time management skills Function effectively with high degree of personal accountability CCRA or SoCRA certified Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Overview
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities
What you will be doing :
Study Planning
- Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion.
- Assume ambassadorial role to facilitate communication between sites and Novartis CPO to increase value proposition to investigators.
- Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the CSM in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
- Negotiate investigator remuneration; prepare financial contracts between investigational sites and investigators. Ensure adherence to payment schedule.
Study Execution
Study Close-out
General
Qualifications
You are :
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 :
Visit our careers website to read more about the benefits of working at ICON :
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 through the form below.
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.
Options
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed