Clinical Research Assistant: Trials Coordination & Data Entry
Illinois Institute of Technology
Illinois Institute of Technology is seeking an individual to assist in various aspects of human clinical trials, including recruiting and scheduling subject visits. The role requires a B.S. degree in Nutrition or related field and offers hands-on experience in a clinical lab environment. Candidates must have strong analytical skills and attention to detail. A competitive benefits package is part of the offer, reflecting the Institute's commitment to employee well-being. #J-18808-Ljbffr
$50k - $52k
...located here: Position Summary Assists with various aspects of human clinical trials with supervision. Aspects of clinical... ..., scheduling subject visits, data entry, quality control, anthropometric... ...Responsibilities Assists with coordination of clinical trials: recruiting,...SuggestedInternshipImmediate start- ...Clinical Research Coordinator Assistant Envisioning and implementing a holistic approach to neurological treatment... ...and identifying participants for trials on site Proactively develops and... .../progress notes, and collects study data via source documents/progress notes...SuggestedTemporary workLocal areaImmediate start
$19.5 - $30.23 per hour
## Clinical Research AssistantApplylocations: Streeterville, Chicago... ...**Job Description**Assists investigators and... ...in the implementation, coordination, and conduct of clinical... ...(consent forms, data collection materials,... ...authorized.* Supports data entry and maintains/updates...SuggestedHourly payFull timePart timeRotating shiftAfternoon shift- ...Clinical Research Coordinators Wanted At Medpace Become a CRA and join our growing team... ...against case report form data, including informing the site staff of any entry errors, ensuring good documentation... ...our integrated Clinical Trial Management System to identify...SuggestedContract workWork at officeRemote workWork from homeHome officeFlexible hours
- ...Clinical Research Associate – Oncology – Chicago ICON plc is... ...or destruction Resolve data queries and drive timely, high‑quality data entry Document site progress... ...to the clinical team Assist in tracking site budgets... ...monitoring Oncology clinical trials required, preferably...SuggestedLocal areaVisa sponsorshipFlexible hours
$91.34k - $114.17k
...Clinical Research Associate - Oncology - Chicago ICON is a... ...destruction Resolve data queries and drive timely, high-quality data entry Document site progress... ...the clinical team Assist in tracking site... ...monitoring Oncology clinical trials required, preferably...Full timeLocal areaVisa sponsorship- Job SummaryClinical Research Coordinators wanted at Medpace! Become... ...based opportunity for clinical research professionals... ...case report form data, including informing the site staff of any entry errors, ensuring good... ...our integrated Clinical Trial Management System to identify...Contract workWork at officeRemote workWork from home
- ...Cincinnati, Ohio!The Clinical Research Associate position offers... ...site staff including coordinators, clinical research... ...against case report form data, including informing the site staff of any entry errors, ensuring good... ...our integrated Clinical Trial Management System to...Contract workWork experience placementWork at officeRemote workWork from home
- ...Clinical Research Associate (Start up) - Cross Therapeutic Area - Illinois... ...be doing? Works on multiple trials within the Cross Therapeutic... ...Operating Procedures (SOPs). Coordinate with the country operations... ...documentation, are met. Possibly assist in audit and inspection...Local areaRemote workWork visaFlexible hours
$91.34k - $114.17k
...Clinical Research Associate (Start up) - Cross Therapeutic Area - IllinoisICON... ...be doing?Works on multiple trials within the Cross Therapeutic... ...Operating Procedures (SOPs).Coordinate with the country operations... ..., are met.Possibly assist in audit and inspection preparations...Local areaRemote workWork visa- ...Medical Laboratory Administrative Assistant About the job Medical... ...accurately and efficiently assist clinical operations. A successful... ...paperwork, performing some data entry, answering phones as needed... ...able to multi-task Able to coordinate multiple projects at once Obsessive...Full timeWork at officeMonday to FridayFlexible hoursWeekend work
- ...Cincinnati, Ohio! The Clinical Research Associate position... ...site staff including coordinators, clinical research physicians... ...case report form data, including informing the site staff of any entry errors, ensuring good... ...our integrated Clinical Trial Management System to identify...Contract workWork experience placementWork at officeRemote workWork from homeHome officeFlexible hours
$50k - $70k
...laboratory does basic, pre-clinical as wellasclinical research.The incumbentshould be a proactive... .... Analyzes and maintains data and/or specimens. Conducts literature reviews. Assists with preparation of reports,... ...data base search and data entry. Ability to be a proactive participant...Contract workWork experience placementFlexible hoursAfternoon shift- ...background in molecular biology to support research on somatic alterations in cancer.... ...position provides hands-on lab work, data collection, and assistive analysis in a dynamic biomedical... ...lab techniques, data collection and entry, and helping prepare reports and manuscripts...
$23.59 per hour
...Sert wants you! The R&D LAB TECHNICIAN is responsible for assisting with day-to-day lab maintenance, formulation preparation and... ...order to conduct sensory panels Process improvement, plant trials, data entry of lab testing, and sensory results for verifying Compile...Hourly payFull timeWork at officeLocal areaLong distance$18.87 - $26.66 per hour
...well as internal equity and industry specific market data. The pay range for each role reflects Rush’s... ...on the circumstances of each case. Summary The Lab Research Assistant 1 performs laboratory support tasks and entry-level scientific procedures under direct supervision...Hourly payFull timeShift work$71.9k - $189k
...Clinical Research MonitorTo be eligible for this position, you must reside in the same country where... ...the study(ies) and reporting study data as required by the study protocol, applicable... ...are available for filing in the Trial Master File (TMF) and verify that the Investigator...Full timePart timeLocal areaImmediate startWorldwide- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job Information Date Opened 12/14/2023 Job Type: Full time... ...Duties And Responsibilities Participate and assist in design and preparation of protocols and case report...Full timeWork experience placement
- ...Clinical Trial Rater – Borderline Personality Disorder (BPD)Location: Remote based in the US Hours... ..., technology solutions, and clinical research services. We collaborate with top pharmaceutical... ...outcomes. Our mission is to combine data science and human expertise to transform...Remote workWorldwideFlexible hours
- ...Clinical Research Associate - Full-Service Syneos Health is a... ...s safety and clinical data integrity at an investigator... ...of the ISF with the Trial Master File (TMF).... ...Site barring you from entry, which could put your... ...when appropriate, to assist employees or applicants...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate- Mid-West ICON plc is a world-leading healthcare intelligence... ...will design and analyse clinical trials, interpreting complex medical data, and contribute to the... ...the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24...Flexible hours
- ...Clinical Research AssociateICON is a global healthcare intelligence and clinical research... ...will design and analyse clinical trials, interpreting complex medical data, and contribute to the... ...and disability coverageEmployee assistance programmes and wellbeing resourcesLearning...
- ...IQVIA seeks a Clinical Trial Rater to conduct standardized psychiatric assessments for a Borderline Personality Disorder study. Remote work... ...validated rating scales, maintain inter-rater reliability, and ensure data quality in line with GCP and study protocol. Required are...Contract workImmediate startRemote work
- ...ICON plc in Chicago is seeking a Clinical Research Associate to serve as the primary liaison between investigational sites and sponsors... ...monitor patient safety, and support site staff training while coordinating with CTAs, LTMs, and CTMs. The ideal candidate has a...
$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. Responsibilities...Remote work$16 - $18 per hour
...Description: Key Responsibilities: Perform specimen sorting, data entry, labeling, imaging, centrifugation, and aliquoting Accurately... ...-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home...Contract workShift workAfternoon shift- ...responsible for receipt, tracking, and entering data into the Laboratory Information... ...accessioning and LIMS / Operation metrics data entry for the Laboratory. This includes working... ...medical terminology applicable to a clinical laboratoryMust be able to perform work with...
- ...numbers as defined by department standards and policies.Updates and/or corrects patient data in various HIM and medical center systems or the physical medical recordCorrects/deletes data entry errors or omissions associated with tasks performed in electronic systemsMaintains...Full timeMonday to FridayShift workDay shiftWeekday work
- ...domain expertise in regulatory sciences, clinical research solutions, quality & compliance,... ...accuracy, completeness, and integrity of the data, and identify and resolve ongoing data issues... .... ~ Monitor assigned clinical trials and clinical sites by reviewing and reporting...Full timeInterim roleWork at officeLocal areaRemote work
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Midwest ICON is a global... ...and monitors clinical trials to ensure sponsor and investigator... ...accuracy of clinical trial data collected, either onsite or... ...disability coverage Employee assistance programmes and wellbeing...Full timeWork experience placementLocal areaRemote workWork visa
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