Clinical Research Associate 2
$91.34k - $114.17kICON
Clinical Research Associate- Mid-WestICON 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 Do:You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: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 reportsYour Profile:You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: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 guidelines.Strong organizational and communication skills, with attention to detail.Ability to work independently and collaboratively in a fast-paced environment.Willingness to travel as required (approximately 60%)Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Rewards & BenefitsICON 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 incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Inclusion and AccessibilityICON 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$91,336.00-$114,170.00
- Clinical Research Associate- Mid-West ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster... ...degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-...SuggestedFlexible hours
$91.34k - $114.17k
Clinical Research Associate - Oncology - ChicagoICON is a global healthcare intelligence and clinical research organisation united by a mission to bring... ...visa sponsorshipA clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical...SuggestedFull timeLocal area$110.52k - $138.15k
Senior Clinical Research Associate - Oncology Phase I - ChicagoICON is a global healthcare intelligence and clinical research organisation united by... ...independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.1+ years early...SuggestedFull timeInterim roleLocal areaRemote work- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job Information Date Opened 12/14/2023 Job... ...RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience...SuggestedFull timeWork experience placement
$57.5k - $226.8k
...accordance with contracted scope of work and Good Clinical Practice.Work with sites to adapt, drive,... ...health care preferred.Requires at least 2 years of on-site monitoring experience.... ...skill in applying, applicable clinical research regulatory requirements. i.e., Good...SuggestedFull timePart timeLocal areaImmediate startWorldwide$96.2k - $151.4k
...site manager throughout all phases of a clinical research study, taking overall responsibility of... ...Regulations, Protocol, Site Monitoring Plan and associated documents.Gains an in-depth... ...5% of working time.Expected travelling ~2-3 days/week.Current driver’s license required...Full timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week$91.34k - $114.17k
Clinical Research Associate (Start up) - Cross Therapeutic Area - IllinoisICON is a global healthcare intelligence and clinical research organisation... ...be located in the Ilinois; near a major airport. Must have 2 -3 years’ experience in monitoring pharmaceutical industry...Full timeLocal areaRemote workWork visa$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... ...Qualifications for the Clinical Research Associate: 2-4 years performing on-site monitoring and...Remote work$91.34k - $114.17k
...Clinical Research Associate (Start up) - Cross Therapeutic Area - IllinoisICON is a global healthcare intelligence and clinical research organisation... ...be located in the Illinois; near a major airport.Must have 2 -3 years' experience in monitoring pharmaceutical industry...Local areaRemote workWork visa- ...Clinical Research Associate - Cross Therapeutic Area - Chicago ICON plc is a world-leading healthcare intelligence and clinical research organization... ...visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical...Local areaVisa sponsorshipFlexible hours
- Job SummaryClinical Research Coordinators wanted at Medpace! Become a... ...exciting home-based opportunity for clinical research professionals with at... ...to fill Clinical Research Associate (CRA) openings with Medpace.... ...Research Coordinator (minimum 2 years)Ability to travel 60-70...Contract workWork at officeRemote workWork from home
$110.52k - $138.15k
Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All RegionsICON 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...Full time- ...Clinical Research Coordinators Wanted At Medpace Become a CRA and join our growing team! This... ...Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our... ...Clinical Research Coordinator (minimum 2 years) Ability to travel 60-70% to...Contract workWork at officeRemote workWork from homeHome officeFlexible hours
- ...Clinical Trial Rater – Borderline Personality Disorder (BPD)Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical... ...in advanced analytics, technology solutions, and clinical research services. We collaborate with top pharmaceutical and biotech companies...Remote workWorldwideFlexible 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...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...ICON plc is seeking a Clinical Research Associate I in Chicago, IL to support clinical trial monitoring across Central/Mid-West regions. You will work with the team to deliver high-quality outcomes, set up studies, monitor progress, and prepare study documentation. Required...
- ...IQVIA seeks a Clinical Trial Rater to conduct standardized psychiatric assessments for a Borderline Personality Disorder study. Remote work in the US, approximately 5 hours per week, start immediate, contract-based engagement. You will administer validated rating scales...Contract workImmediate startRemote work
$25 - $28 per hour
...Profit sharing Retirement plan The Clinical Research Assistant will play a crucial role in... ...School Diploma or equivalent required. Associate's degree or higher in a related field (... ...% to 66% 26-50 lbs. Occasionally from 2% to 33% Pushing/Pulling Frequency...Full timeImmediate startMonday to Friday$160k - $200k
...compensation types Annual Bonus and RSUs Site Director, Clinical Operations (CRA) - Midwest Region Remote from Chicago, IL, Minneapolis... ...and inclusivity. Seniority level Mid-Senior level Employment type Full-time Job function Research #J-18808-LjbffrPermanent employmentFull timeContract workLocal areaRemote work- ..., building strong relationships with investigators and site staff Identify and resolve site-level issues, escalating risks to the Clinical Team Lead/PM as appropriate Review and ensure completeness of essential documents/TMF in line with ICH-GCP and company SOPs Support...Remote work
- ...Clinical Research Associate AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key...Contract workTemporary workLocal area
- ...Join Our CRA Team in Cincinnati, Ohio!The Clinical Research Associate position offers an exciting career within clinical research! For those with Life Science PhD backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical...Contract workWork experience placementWork at officeRemote workWork from home
- ...Senior Clinical Research Associate - Oncology Phase I - Chicago ICON plc is a world-leading healthcare intelligence and clinical research organization... ...conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials. ~1+ years...Remote jobInterim roleLocal areaFlexible hours
- Responsibilities include site evaluation, training, ongoing monitoring, and leveraging CRM tools to drive performance while maintaining compliance with GCP and regulatory standards. Travel requirements up to 75% are anticipated as part of site management. #J-18808-Ljbffr...
- ICON plc is a world-leading healthcare intelligence and clinical research organization. This Clinical Research Associate II role in the Midwest involves designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments...
- ...Research Technician The Chevrier Lab is seeking a Research Technician with a background... ...immunology techniques in vitro and in vivo, (2) next-generation sequencing-based... ...technical duties in a laboratory doing non-clinical as well as clinical research, carrying out...TraineeshipWork experience placement
$50k - $70k
...assist with the daily technical and project associated duties. The laboratory does basic, pre-clinical as well as clinical research. The incumbent should be a proactive participant... ...related fields. Experience: ~1-2 years of experience in a research environment...Contract workWork experience placementFlexible hoursAfternoon shift- AbbVie is seeking a Clinical Research professional to advance clinical trials by engaging investigators, training site staff, and monitoring site performance with a strong focus on data integrity and patient safety. You will partner with sites to ensure compliant trial...
$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- ...Miscellaneous Perform other duties as assigned Minimum Qualifications: ~ A high school diploma or its equivalent along with 2 years of administrative support experience is required. Minimum Competencies: Excellent written and verbal communication...Work at office
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