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Clinical trial manager Jobs in Topeka ks
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Clinical Trial Manager
VirtualVocationsTopeka, Kansas, United StatesAssistant Clinical Director
Ascend Hospice & Palliative Care KSTopeka, Kansas- Promoted
Clinical and Forensic Sales Manager - Central
Waters CorporationKS, US- Promoted
SENIOR RX CLINICAL PROGRAMS PHARMACIST
CenterWellTopeka, KS, United States- Promoted
- New!
CLINICAL PSYCHOLOGIST (PUBLIC NOTICE FLYER)
HQDA Field Operating Agencies and Staff Support AgenciesKS, United States- Promoted
- New!
REMOTE ASSOCIATE CLINICAL DIRECTOR | WFH
Get It Educational ServicesKS, United States- Promoted
- New!
Clinical Pharmacist
Ardent HealthTopeka, KS, United States- Promoted
Trial Court Clerk II - 3rd Judicial District
Kansas Judicial BranchTopeka, KS, US- Promoted
Director, Clinical Services
Pathway Family Services LLCTopeka, KS, US- Promoted
Clinical Pharmacist PRN
AdventHealthTopeka, KS, United StatesClinical Case Manager BH Field
CVS HealthKansas, US- Promoted
Clinical Supervisor
TFI Family Services, Inc.Topeka, KS, United States- Promoted
Clinical Research Coordinator
Barrington JamesKS, United StatesBehavioral Health Program Manager (Clinical Therapist Supervisor) (AAC)
State of KansasMiami, Kansas, US- Promoted
Clinical Program Manager - CCBHC
Sunflower Health PlanKS, United StatesClinical Dietitian - Clinical Nutrition - FT - Day
Stormont Vail HealthTopeka, KSClinical Trial Manager
VirtualVocationsTopeka, Kansas, United States- Full-time
A company is looking for a Clinical Trial Manager to oversee and ensure the successful delivery of clinical trials.Key ResponsibilitiesDeliver trials on time, within budget, and with high qualityManage the evaluation and selection of investigative sites and vendorsDevelop and manage trial timelines, budgets, and recruitment plansRequired QualificationsBS / BA degree or relevant degree with a strong emphasis on scienceMinimum of four years of experience in the biopharmaceutical industry or relevant clinical researchOncology experience is required; dermatology experience is a plusWorking knowledge of ICH Good Clinical Practices and relevant regulatory experienceExperience in executing a wide range of clinical trial activities from initiation to reporting