6 clinical trial manager jobs at 3 companies in Berkeley, MO
2d
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Manager Clinical Trials (Hybrid) - Radiology
St. Louis, Missouri, United States
$75k-$129k/yr HybridFull Time
1+ YOEBachelor’s degree or equivalent education and experience, plus at least one year of clinical research experience. Leadership, clinical trials administration, budgeting, regulatory compliance, and Microsoft Office skills preferred.
Microsoft Excel, Microsoft Word, SQL
3w
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Clinical Research Financial Coordinator II - Cardiology
Saint Louis, Missouri, United States
$53k-$91k/yr OnsiteFull Time
2+ YOEBachelor's degree (or equivalent experience), minimum 2 years clinical trials and 2 years finance/business management experience; strong billing compliance, budgeting, and financial analysis skills.
Database Software, Spreadsheets, Computer Applications
1mo
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Assistant Professor of Medicine - Oncology
St. Louis, Missouri, United States
OnsiteFull Time
Clinical-track oncology faculty to provide outpatient genetics and inpatient hematologic malignancy care, supervise trainees, support clinical trials, and participate in teaching and committees.
1mo
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Research Nurse Coordinator II - Gastroenterology (IBD)
Saint Louis, Missouri, United States
$65k-$110k/yr OnsiteFull Time
2+ YOEAssociate degree or nursing diploma, active RN, BLS required, 2+ years research and nursing experience, clinical trials management, EHR and database familiarity, phlebotomy and GCP/IATA preferred.
Electronic Health Records (EHR), SAS, Spreadsheet Software
3mo
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Chief, Gynecologic Radiation Oncology and Brachytherapy
St. Louis, Missouri, United States
OnsiteFull Time
MD with board certification in Radiation Oncology, expertise in interstitial and intracavitary HDR brachytherapy and MRI-guided adaptive radiotherapy, leadership and academic productivity with clinical trial experience.
MRIdian, Varian Ethos, Hypersight, MRI
1d
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Principal Investigator
St. Louis, Missouri, United States
HybridPart Time
2+ YOEMD or DO required; related PhD may be considered. Requires GCP certification and 2+ years as a Principal or Sub-Investigator in clinical trials; board certification preferred.
FDA Form 1572, Standard Operating Procedures (SOPs), ECG, Clinical Study Reports, Case Report Forms (CRFs)