- ICON Clinical Research (Lenexa, KS)
- Clinical Data Quality Associate - US, Lenexa, KS - On-Site ICON plc is a world-leading healthcare intelligence and clinical research organization. ... or secondary vocational education required + 1-2 years work experience in quality control, data entry, or clinical research preferred **Benefits of Working… more
- Philips (Lenexa, KS)
- ** Clinical Research Associate (Remote-Home Based)** Together with the Clinical Operations Manager, you will support the execution Clinical Trials for the ... and qualification, and initiation. As well, developing the monitoring plan for clinical studies. + Supporting electronic data capture (EDC) user acceptance… more
- IQVIA (Overland Park, KS)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be ... initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.… more
- IQVIA (Overland Park, KS)
- …work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (Overland Park, KS)
- …work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...manage ongoing project expectations and issues. * Evaluate the quality and integrity of study site practices related to… more
- IQVIA (Overland Park, KS)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines +… more
- IQVIA (Overland Park, KS)
- **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 and adhere to all ... selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. +… more
- IQVIA (Overland Park, KS)
- …plus administering protocol and related study training to assigned sites + Evaluating the quality and integrity of site practices - escalating quality issues as ... regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable...will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A… more
- IQVIA (Overland Park, KS)
- …plus administering protocol and related study training to assigned sites + Evaluating the quality and integrity of site practices - escalating quality issues as ... by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and… more
- Eurofins (Lenexa, KS)
- …discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract ... Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years,… more
- AdventHealth (Shawnee, KS)
- …The Clinical Documentation Specialist (CDS) is part of the Quality Management department. The CDS assists physicians and other healthcare providers in ... each position may vary based on geographical location. **Category:** Quality / Clinical Effectiveness **Organization:** AdventHealth Shawnee Mission **Schedule:**… more
- US Tech Solutions (Kansas City, MO)
- …study. + The Sr. CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity, quality , and timely ... Administration (FDA), Clinical Trials. **Education:** + High School Diploma or associate degree. **About US Tech Solutions:** US Tech Solutions is a global staff… more
- Eurofins (Lenexa, KS)
- …teams as requested by supervisory staff. Level I - Minimum + BS or BA in Clinical Laboratory Science + OR Associate 's in Medical Laboratory Technician + OR BS or ... discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract… more
- CenterWell (Kansas City, MO)
- …a part of our caring community and help us put health first** The ** Clinical Manager** coordinates and oversees all direct care patient services provided by ... clinical personnel. + Develops, plans, implements, analyzes, and organizes clinical operations for a specific location managed. + Conducts/delegates the… more
- Medtronic (Kansas City, KS)
- …expectations by striving without reserve for the greatest possible reliability and quality in our products, processes, and systems by being accountable, having a ... voice and taking action. Clinical Specialists are required to be within their assigned...complex mathematics, mechanical concepts, science or computing -OR- + Associate 's Degree PLUS a minimum 4 years of work… more
- Catalent Pharma Solutions (Kansas City, MO)
- ** Associate Scientist II, Biologics II** **Position Summary** **:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical ... lives. Catalent's Kansas City facility is home to our Clinical Delivery Services and Biologics Analytical Services businesses. The...Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II for Biologics III who is responsible… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Position Summary:** Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II for our Biologics II Team. The main activities will be to ... provide and report data , as required by project contracts within the Biologics...submission in Regulatory packages, release and stability testing of clinical and animal trial dose forms and in support… more
- Eurofins (Lenexa, KS)
- …of possible compliance issues and suggests/facilitates corrective actions. + Hosts Monthly Clinical Quality Meeting and supports Quality Council meetings ... the direction of the Clinical Laboratory Director and Director of RA/QA, the Quality Manager will implement and perform functions in support of the Quality … more
- Eurofins (Lenexa, KS)
- …Biostatistics Analyst is primarily responsible for applied statistics in support of clinical data analysis plus new assay/method, design and validation efforts ... - Minimum + Provide biostatistical support for R&D projects requiring statistical analysis of clinical data , and programming and handling omics data . + Work… more
- Eurofins (Lenexa, KS)
- …issues or discrepancies. + Complete correction requests as needed. + Adhere to all Data Management policies and protocols. + Maintain quality control and ... forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global...primarily responsible for performing duties related to accessioning and data entry with a high degree of proficiency. Essential… more