- Edwards Lifesciences (Topeka, KS)
- …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
- Parexel (Topeka, KS)
- …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
- Parexel (Topeka, KS)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Topeka, KS)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Topeka, KS)
- The Manager , Central Monitoring is accountable for centralized monitoring activities for global and/or complex trials, analytical data review of key risk ... data and presenting as an integral member of the Clinical Study team for clinical development studies....interpreted, reported and presented to the study teams. The Manager , Central Monitoring , will be responsible for… more
- Merck (Topeka, KS)
- …or business management is preferred. **Prerequisites:** + Minimum of 6 years in clinical research including at least 2 years with developing and managing ... up of regulatory inspections. **Operational Quality Management:** + The Clinical Quality Operations Manager is accountable for... Clinical Data Management, Clinical Development, Clinical Quality Management, Clinical Research ,… more
- Otsuka America Pharmaceutical Inc. (Topeka, KS)
- …sciences or related field; advanced degree a plus. + 6-8 years of experience in clinical quality assurance or clinical research within the pharmaceutical or ... **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the...of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good … more
- Parexel (Topeka, KS)
- …or equivalent. + **Experience:** 3-5 years of relevant industry experience ( clinical research , feasibility, site engagement, project coordination, or related ... **PXL FSP - Join an organization shaping smarter, faster clinical development** PXL FSP is seeking a detail‑oriented and proactive **Feasibility Study Manager **… more
- ICON Clinical Research (Lenexa, KS)
- …Part-Time; Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ... us on our mission to shape the future of clinical development. We are currently seeking an Environmental, Health...are currently seeking an Environmental, Health & Safety (EHS) Manager to join our diverse and dynamic team. As… more
- Sumitomo Pharma (Topeka, KS)
- …diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more ... across the SMPA organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and… more
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