Clinical Research Associate
$91.34k - $114.17kIcon Clinical Research
Clinical Research Associate - Midwest 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. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What you will be doing * Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced
- Experience in ophthalmology or gene therapy studies
- Ability to travel at least 60% of the time (international and domestic - fly
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career
- Position Title: Clinical Research Associate Location: Grayslake, IL, 60030 Duration: 1 Year (Possible Extension) Work Arrangement: 100% Onsite Schedule: PM weekdays and available weekends post-training Department: Clinical Pharmacology & Pharmacometrics Research...SuggestedWeekend workWeekday work
- ...Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials. You will collaborate closely with cross‑functional teams to ensure adherence...SuggestedInterim roleLive inLocal areaRemote work
$100k - $120k
...Piper Companies is currently seeking aClinical Research Associate (CRA) for an opportunity in Chicago, Illinois (IL).The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization....SuggestedRemote work$71.9k - $189k
...out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. • i.e., Good Clinical Practice (GCP)...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...entry Document site progress and elevate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site... ...work in the United States without visa sponsorship A clinical research professional with 2+ years of on‑site monitoring experience in...SuggestedLocal areaVisa sponsorshipFlexible hours
- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$120k - $135k
...Piper Companies is actively seeking Clinical Research Associates to join a toptier CRO with a proven track record of excellence, trusted by global pharma and biotech partners. This position is fully remote but does require travel 60-80% of the time regionally with...Remote work- Clinical Research Associate - Oncology - Chicago 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...Local areaVisa sponsorshipFlexible hours
- ...Clinical Research Associate - Early Development Multi Therapeutic - Midwest Region 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...Local areaVisa sponsorshipFlexible hours
- ...CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the...Local areaRemote workFlexible hoursShift work
- ...Chicago, United States | Posted on 12/27/2024 Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Participate and assist in design and...
- ...site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports... ..., resources and timelines Qualifications 5+ years of clinical research monitoring experience (including pre-study, initiation, routine...
$66.8k - $120k
...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs...Temporary workWork at officeRemote workHome officeFlexible hoursNight shift$100k - $120k
...Piper Companies is seeking an Oncology Clinical Research Associate to support a leading organization within the clinical trials industry in Chicago, IL . The Oncology Clinical Research Associate will play a vital role in managing investigative sites and ensuring the successful...Remote work- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol...For contractorsLocal areaRemote work2 days per week3 days per week$101.6k - $169.3k
...Job Overview IQVIA is hiring Senior Clinical Research Associate 1 with experience in oncology, cardiovascular, renal, metabolic, CNS, obesity (GLP‑1), diabetes, GI, MASH/NASH, dermatology, or respiratory. Perform monitoring and site management work to ensure that sites...Full timePart timeLocal areaImmediate start- ...A Senior Clinical Research Associate (Sr. CRA) is responsible for: Key Responsibilities Conducting monitoring activities at assigned clinical trial site(s) Verifying the adequacy, reliability, and quality of data collected at clinical sites Ensuring the conduct of the...Fixed term contractInterim roleLocal areaWork from home
$78k - $130k
...Positions available: 1 (remote based, Canada) Must be fluent in English and French. Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational...Remote workWork from home- A leading clinical research company is seeking a Lead Clinical Research Associate (CRA) to manage full site monitoring services. The ideal candidate must be fluent in English and French and possess a college degree along with 4-6 years of experience. Responsibilities include...Remote workWork from home
- ...CRA Team Opportunity in Cincinnati, Ohio Join our CRA Team in Cincinnati, Ohio! The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference...Contract workWork experience placementWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Springfield, Illinois. The Sr. CRA will manage site monitoring and ensure quality study execution. Responsibilities include overseeing clinical trial activities, resolving protocol-related issues, and...Remote work
- ...Job Purpose Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry‑leading performance. Partner with investigators and site staff for meaningful...Contract workTemporary workLocal areaRemote work
- ...A leading clinical research organization in Chicago is seeking a Clinical Research Associate to provide essential support for clinical trials. This role involves assisting with the design and preparation of clinical protocols, generating standard operating procedures,...
$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...laws & regulations, protocol, site monitoring plan and associated documents. Gains an in‑depth understanding of the study protocol...Remote jobLocal areaRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week$65k - $75k
The Clinical Research Associate (CRA) role focuses on supporting clinical trials, regulatory submissions, and ensuring compliance with relevant clinical regulations and industry standards. The primary responsibilities include managing study tracking tools, documentation...Full timeWork at officeLocal areaImmediate startRemote work- Merck & Co. is seeking a qualified candidate to oversee site management for clinical research programs. The role emphasizes ensuring compliance with ICH-GCP and country regulations, acting as primary site contact, and expanding the site network across assigned territories...
$50k - $52k
...well-being is reflected in our competitive benefits package located here: Position Summary Assists with various aspects of human clinical trials with supervision. Aspects of clinical trials include recruiting, screening, enrollment, scheduling subject visits, data entry...InternshipImmediate start$19.5 - $30.23 per hour
...Hospital of Chicago Job Description Assists investigators and study team in the implementation, coordination, and conduct of clinical research activities. Adheres to the service values and principles as well as the principles of research ethics. Essential Job Functions...Hourly payFlexible hoursRotating shiftAfternoon shift$19.23 - $24.04 per hour
...About The Department BSD OCR - Clinical Research Incubation Office of Clinical Research (OCR) is the nucleus of the clinical research enterprise, providing services, training, tools and compliance oversight to support the conduct of clinical research across the entire...Hourly payWork experience placementWork at office
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