Clinical Research Assistant: Data Entry & Coordination
$30 per hourSPECTRAFORCE
A healthcare 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 candidate has a BS/BA in life sciences, basic knowledge of clinical trials, and proficiency in MS Office applications. Responsibilities include data entry, scheduling visits, and maintaining study documentation. The position offers a pay rate of $30.00/hr along with a contract employment type. #J-18808-Ljbffr SPECTRAFORCE
- Clinical Research Assistant - ONC Radiation Oncology page is loaded## Clinical Research... ...Assistant assists in entry level clinical research activities... ...to assist in coordination of all aspects of clinical... ...screening for eligibility, data entry, maintenance of regulatory...SuggestedHourly payFull timeWork experience placement
$22.88 - $33.17 per hour
The Clinical Research Assistant assists in entry level clinical research activities. Under general supervision, the... ...CRO representatives to assist in coordination of all aspects of clinical... ...recruitment, pre-screening for eligibility, data entry, maintenance of regulatory...SuggestedHourly payFull timeWork experience placement- Clinical Research Lead Assistant Join ICON Strategic Solutions as a Clinical Research Lead Assistant. ICON... ..., SharePoint, Lists, Forms, etc.) Coordinate and schedule internal and external... .../ Investigator Engagement (e.g., data entry, troubleshooting, etc.) Support retention...SuggestedFull timeFlexible hours
$25 - $39 per hour
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...SuggestedHourly payPart time$30 per hour
...study supplies, EDC entry/query resolution, visit... ...Summary A typical Research Assistant performs a variety of... ...tasks in support of clinical trials and assists in... ...procedures to collect data on patients enrolled... ...g. clinical research coordinator, nurse, medical assistant...SuggestedContract workWork experience placementLocal area$78k - $130k
...deliver and/or perform full clinical site monitoring services for... ...site/patient recruitment, site data/document management, monitoring... ...to manager for peers. Assist with selection, hiring, training... ...recruit site investigators, coordinate the movement and delivery of...Remote workWork from home$66.8k - $120k
...Description Join Us as a Clinical Research Associate (Level II) – Make... ...opportunity to perform and coordinate all aspects of the clinical... ...subjects' 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- ...Certified Phlebotomist/Lab Assistant Encompass Medical... ...a pivotal role in coordinating activities between out-patients, outlying clinics, and laboratory personnel... ...all pertinent patient data Collects appropriate... ...laboratory Performs data entry of patient information...Full timeWork at officeRelocation package
- ...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
$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... ...involves assisting with clinical trials, patient recruitment, and data management while collaborating with healthcare...Hourly payFull time$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$17 - $20 per hour
...opportunities for growth!! We are looking for entry level candidates for positions in our... ...using standard techniques Calculating data Recording and reporting data and any unusual... ...or verbal instructions Cooperate and coordinate both orally and in writing Able to follow...Full timeDay shift- ...Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare... ...trials, interpreting complex medical data, and contributing to the advancement of... ...for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour...Flexible hours
$47.4k - $169.3k
...conducting the study(ies) and reporting study data as required by the study protocol,... ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...and skill in applying, applicable clinical research regulatory requirements (i.e., Good...Full timePart timeLocal areaImmediate startWorldwide$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. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house monitoring experience. Candidates...Full timePart timeLocal areaImmediate startWorldwide- ...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
$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly... ..., enrollment, case report form (CRF) completion, and data query resolution. Support the start-up phase as required....Full timePart timeLocal areaImmediate startWorldwide- Clinical Research Associate - Multi TA ICON plc is a world-leading healthcare intelligence and... ...success of clinical trials by ensuring data integrity, participant safety, and... ...the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour...Flexible hours
$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience... ...that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and...Full timePart timeLocal area- ...Lab Assistant Position Labcorp is seeking a Lab Assistant to join our team in the Anatomic... ...Job Responsibilities Receive and sort clinical lab specimens Prepare specimens for testing and analysis Scan and/or data entry of specimen and patient information...Daily paidTemporary workCasual workReliefInternshipFlexible hours
- ...Lab Assistant Eurofins Viracor LLC is an equal opportunity employer and encourages individuals... ...management, problem resolution, and data entry and specimen storage with a high degree... ...or equivalent required ~2 years of clinical laboratory experience preferred ~ Must...Full timeTemporary workWork at officeVisa sponsorshipWork visaWeekend workAfternoon shift
- ...as required. Demonstrates good laboratory practice. May also coordinate the activities of the lab. Responsibilities Reports and maintains... ...Retirement Contribution 401(k) plan with BJC match Tuition Assistance available on first day BJC Institute for Learning and...Full timeRelocation packageFlexible hoursShift workWeekend work
- ...pediatric patients in a collaborative clinical environment. Preferred... ...admission activities, and order entry processing. Responsibilities... ...perform various waived testing. Assists in problem requisitions/... ...machinery, etc. Frequent keyboard use/data entry. Occasional bending,...Hourly payWork experience placementMonday to FridayFlexible hoursShift workDay shift
- ...development of treatments that benefit patients worldwide. Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON... ...plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development...Worldwide
- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical... ...plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global...Flexible hours
$71.9k - $189k
IQVIA is looking for a Site Monitor in Overland Park, Kansas. The role involves site management and monitoring to ensure compliance with protocols and regulations. Candidates should have at least 2 years of monitoring experience and preferably a Bachelor's Degree in a scientific...Work at office- Overview Experienced Clinical Research Associate - Full-Service Syneos Health... ...\'s safety and clinical data integrity at an investigator/... ...result in a Site barring you from entry, which could put your ongoing... ..., when appropriate, to assist employees or applicants to perform...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...$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase... ...We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play... ...integrity and quality of clinical research data. Key Responsibilities Conduct all types...Full timePart time- ...Clinical Research Associate, Sponsor Dedicated Overland Park, United States of America | Full time | Field-based | R1541497 Perform monitoring... ...that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and...Full timeLocal area
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