Clinical Research Assistant - Cardio Trials & Data Entry
$25 - $39 per hourIQVIA
A clinical research organization is seeking a Site Research Assistant in Kansas City, MO, to support clinical trial activities. Responsibilities include data entry, chart reviews, and managing participant schedules while ensuring protocol compliance. Candidates should have an associate’s degree and a minimum of one year of relevant experience, demonstrating strong attention to detail and organizational skills. This is a part-time, on-site role with a pay range of $25.00 to $39.00 per hour. #J-18808-Ljbffr IQVIA
$22.88 - $33.17 per hour
The Clinical Research Assistant assists in entry level clinical research activities. Under general supervision, the... ...recruitment, pre-screening for eligibility, data entry, maintenance of regulatory... ...of patients regarding clinical trials following established procedures...SuggestedHourly payFull timeWork experience placement$30 per hour
...staffing organization is seeking a Research Assistant in Kansas City, MO. This role involves supporting clinical trials by performing various administrative tasks to collect data on patients. The ideal... ...Responsibilities include data entry, scheduling visits, and maintaining...SuggestedContract work- Clinical Research Assistant - ONC Radiation Oncology page is loaded## Clinical Research... ...Assistant assists in entry level clinical research activities... ...-screening for eligibility, data entry, maintenance of... ...therapies, cutting-edge clinical trials and world class research. Radiation...SuggestedHourly payFull timeWork experience placement
- ...benefit patients worldwide. Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON... ...and sites. Well‑versed in clinical trial management. They are rigorous,... ...assurance and disability coverage Employee assistance programmes and wellbeing resources...SuggestedWorldwide
- Clinical Research Lead Assistant Join ICON Strategic Solutions as a Clinical Research Lead Assistant. ICON plc is a world-leading... ...Provide administrative support for clinical trials / Investigator Engagement (e.g., data entry, troubleshooting, etc.) Support retention‑...SuggestedFull timeFlexible hours
- A leading clinical research organization in Overland Park is seeking a Clinical Research Technician II to execute clinical trial activities while ensuring compliance with study protocols and maintaining participant confidentiality. The ideal candidate will have a High...
$30 per hour
...Maintain study supplies, EDC entry/query resolution, visit... ...portals Summary A typical Research Assistant performs a variety of administrative... ...tasks in support of clinical trials and assists in the performance... ...clinical procedures to collect data on patients enrolled and/or...Contract workWork experience placementLocal area- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare... ...and sites. Well‑versed in clinical trial management. They are rigorous,... ...the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour...Flexible hours
$22.88 - $33.17 per hour
...University of Kansas Medical Center is seeking a full-time Clinical Research Assistant for the Radiation Oncology department in Kansas City. This role involves assisting with clinical trials, patient recruitment, and data management while collaborating with healthcare...Hourly payFull time$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have... ...conducting the study(ies) and reporting study data as required by the study protocol,... ...documents are available for filing in the Trial Master File (TMF) verify that the...Full timePart timeLocal areaImmediate startWorldwide$78k - $130k
..., deliver and/or perform full clinical site monitoring services for one... .../patient recruitment, site data/document management, monitoring... ...feedback to manager for peers. Assist with selection, hiring,... ...the movement and delivery of trial materials, samples, tests and...Remote workWork from home$71.9k - $145.3k
...Study Start-Up Clinical Research Associate IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams... ...activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with monitoring procedures and...Full timePart timeLocal areaImmediate startWorldwide- ...Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading... ...designing and analyzing clinical trials, interpreting complex medical data, and contributing to the... ...years ahead. Global Employee Assistance Programme, TELUS Health, offering...Flexible hours
$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you'll play a crucial role... ...case report form (CRF) completion, and data query resolution. Support the start-up phase... ...all site documents are filed in the Trial Master File (TMF) and Investigator's Site...Full timePart timeLocal areaImmediate startWorldwide- Clinical Research Associate - Multi TA ICON plc is a world-leading healthcare... ...and managing clinical trial activities to ensure they are... ...clinical trials by ensuring data integrity, participant... ...ahead. Global Employee Assistance Programme, LifeWorks, offering...Flexible hours
$66.8k - $120k
...Description Join Us as a Clinical Research Associate (Level II) – Make... ...biotechs, spanning 2,700 clinical trials across 100+ countries in the... ...' rights, well-being, and data reliability. You will ensure... ...to the project team by assisting in preparation of project publications...Temporary workWork at officeRemote workHome officeNight shift$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have... ...conducting the study(ies) and reporting study data as required by the study protocol,... ...documents are available for filing in the Trial Master File (TMF) verify that the...Full timePart timeLocal area- ...microscopic, and bacteriologic tests to obtain data for use in diagnosis and treatment of... .... Performs periodic maintenance and assists with the calibration of instruments. Assists... ...machinery, etc. Frequent keyboard use/data entry. Occasional bending, stooping, kneeling,...Hourly payFlexible hoursShift workNight shift
- ...Senior Clinical Research Associate, Early Clinical Development Kansas City, United States of America... ...the successful execution of clinical trials. In this position, you will be... ...integrity and quality of clinical research data. Key Responsibilities Conduct all...Full time
- ...Clinical Research Associate, Sponsor Dedicated Overland Park, United States of America | Full... ...conducting the study(ies) and reporting study data as required by the study protocol,... ...documents are available for filing in the Trial Master File (TMF) and verify that the Investigator...Full timeLocal area
$22.88 - $33.17 per hour
The University of Kansas Medical Center is hiring a Clinical Research Assistant for full-time hours in Kansas City, Missouri. Responsibilities include assisting with patient recruitment, managing clinical data, performing study procedures, and ensuring compliance with regulatory...Hourly payFull time- Overview Experienced Clinical Research Associate - Full-Service... ...s safety and clinical data integrity at an... ...contents 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
$71.9k - $169.3k
IQVIA Argentina is hiring a Clinical Research Associate in Overland Park, Kansas. The role includes monitoring and managing clinical trial sites to ensure compliance with protocols and regulations. Ideal candidates should have 1-2 years of experience in clinical research...- ...performing duties related to accessioning and data entry with a high degree of proficiency.... ...activities efficiently. Maintain other Clinical Laboratory databases as needed or... ...daily workload as required. Ability to assist Management in providing overall direction...Full timeWork at officeVisa sponsorshipWork visaWeekend workAfternoon shift
- ...you will oversee and manage clinical trial activities to ensure they are... ...seeking a Lead Clinical Research Associate (CRA) to join our... ...ensuring the highest levels of data quality and patient safety.... ...disability coverageEmployee assistance programmes and wellbeing resources...Worldwide
- A leading clinical research organization is seeking a Clinical Research Associate dedicated to supporting clinical trials. The ideal candidate should have 1-2 years of onsite monitoring experience, a bachelor's degree in a scientific discipline, and a strong understanding...
- A leading healthcare organization in Kansas City is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities ensuring compliance with protocols and quality standards. The ideal candidate will possess an advanced degree, extensive CRA experience...
$20 per hour
...accurate and timely reporting of analytical data. The position operates within a 24-hour... ...glassware, maintain laboratory cleanliness, and assist with general housekeeping to support safe... ...laboratory workflows. Complete data entry for metrics and key performance indicators...Contract workTemporary workImmediate startShift workRotating shiftDay shiftAfternoon shift$29 - $41 per hour
...Technologist I'm hiring for a Med Tech in Kansas! There is potential for 5k relocation assistance. The Med Tech perform pre-analytic testing responsibilities including clerical duties, data entry, specimen collection, and specimen processing; performs waived, moderate...Permanent employmentFull timeRelocation packageShift workNight shift- ...A prominent healthcare organization is seeking a remote Clinical Research Associate (CRA) to manage clinical site monitoring services for various projects. The role requires fluency in both English and French, with a focus on site recruitment, oversight of project budgets...Remote work
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