- Parexel (Topeka, KS)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Topeka, KS)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Topeka, KS)
- …Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + ... + Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction, investigational product(s),… more
- Parexel (Topeka, KS)
- …champion, etc.). **Skills:** + Strong understanding of the different operational aspects of clinical study conducts in different regions across the world, which ... **Homebased US** As a Proposal Manager with Parexel you are in a client...(RFP) process + Receives and analyzes RFP documentation including study protocol or synopsis and ensures all appropriate Subject… more
- Parexel (Topeka, KS)
- …champion, etc.). **Skills:** + Strong understanding of the different operational aspects of clinical study conducts in different regions across the world, which ... **US Homebased** A Contracts Manager with Parexel is a client facing role and requires consistent management of the contract management processes, development of… more
- Parexel (Topeka, KS)
- …assigned project/ study . + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), ... Supporting Activities - Medical Support / Medical Monitoring for projects and studies contracted to Parexel - Deliver all medical support required for successful… more
- Parexel (Topeka, KS)
- …management activities **CSR Narratives (as applicable)** + Performing medical review of Clinical study report narratives according to the client's guidelines and ... and sign off adverse events report for accuracy and clinical importance, relationship to the study drug...processing cycle + Provide input as necessary to Feasibility Studies , Data Monitoring Committees (DMCs), Clinical Endpoint… more
- Parexel (Topeka, KS)
- …investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical ... /scientific writing skills. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or… more
- Parexel (Topeka, KS)
- …practice + Interact with clients and regulatory authorities + Review publications and clinical study reports + Travel to, attend, and actively contribute to ... discussing study results) + Additional responsibilities as defined by supervisor/ manager . **Skills:** + Good analytical skills + Good project management skills +… more
- Parexel (Topeka, KS)
- …Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead ... providing client liaison and proposals input. **Key Accountabilities** : **Author Clinical Documents** + Gather, review, analyze, and evaluate pertinent resources to… more
- ICON Clinical Research (Lenexa, KS)
- Clinical Study Manager - Lenexa, KS (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to ... us on our mission to shape the future of clinical development. At ICON, it's our people that set... study management or director of operations, the study manager will be responsible for the… more
- Oracle (Topeka, KS)
- …across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical ... Failure Mode and Effects Analyses (FMEAs), hazard analyses, and usability studies for clinical safety. . Partner with engineering teams to identify and mitigate… more
- Oracle (Topeka, KS)
- …across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical ... Failure Mode and Effects Analyses (FMEAs), hazard analyses, and usability studies for clinical safety. . Partner with engineering teams to identify and mitigate… more
- IQVIA (Overland Park, KS)
- …Job Overview Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained ... of resources to clinical research projects by assigning staff to clinical studies based on their experience and training. * Manage the quality of assigned… more
- Mental Health Association of SCK (Wichita, KS)
- …provision, ethics and professional development. + Works with Senior Director/Billing Manager / Clinical Coordinator to ensure effective and efficient front office ... POSITION TITLE : Clinical Director of Outpatient and Addiction Services FLSA...and possess independent licensure in their respective field of study and with a minimum of two years' experience… more
- IQVIA (Overland Park, KS)
- 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 ... SSO Study Start-Up Team Lead, the SSO Study Start-Up Manager , and the SSO Feasibility...sponsor strategy IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to… more
- Oracle (Topeka, KS)
- …combined higher education and related work experience including: + Bachelor's degree in Nursing, Clinical Studies , Health Care, or related field + At least 1 ... , ShiftAlert, Demand Manager , Outcomes-Driven Acuity, and Patient Progress Manager . **Responsibilities** As a Senior Clinical Consultant, you will partner… more
- Edwards Lifesciences (Topeka, KS)
- …small medical writing team to support clinical and regulatory submissions (eg, clinical study reports, clinical evaluation reports) and may indirectly ... expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of...and be part of our inspiring journey. The Senior Manager , Medical Writing oversees medical writing projects and team… more
- Wolters Kluwer (Wichita, KS)
- …(see locations listed on the posting) **OVERVIEW** The Customer Success Engagement Manager plays a high-impact role in managing strategy and product utilization ... across the Wolters Kluwer Health's Clinical Decision Support & Provider Solutions (CDSP) product portfolio....utilization goals and benchmark success, leveraging tools (reports, case studies , client references, etc.) to win and maintain customer… more
- Otsuka America Pharmaceutical Inc. (Topeka, KS)
- …Drug Product and Final Packaged/Labeled Investigational Medicinal Product) for use in clinical studies and commercial products. + Works collaboratively with GMP ... The Senior Manager , Global Product Quality - Biologics is responsible...as applicable in releasing R&D products for use in clinical studies and commercial supply. + Reviews/approves… more
