4 trial manager jobs at 4 companies in Arkansas
1w
Save
Mark Applied
Hide
Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only)
United States or North Carolina or Rhode Island or Maine or Ohio or Arizona or Delaware or Tennessee or Louisiana or Maryland or Michigan or Colorado or Connecticut or District of Columbia or Hawaii or North Dakota or New York or Virginia or Georgia or Wisconsin or New Hampshire or Arkansas or Vermont or Mississippi or Alaska or Washington or Montana or Missouri or Texas or Kansas or Illinois or Oklahoma or California or Nevada or Florida or West Virginia or Idaho or Pennsylvania or Indiana or Nebraska or Utah or New Mexico or New Jersey or South Dakota or Kentucky or South Carolina or Alabama or Wyoming or Massachusetts or Minnesota or Puerto Rico or Iowa or Oregon
RemoteFull Time
3+ YOERequires 3+ years of clinical project management, full trial lifecycle experience, Phase 2b inflammation experience, CRO/vendor oversight, cross-functional leadership, and knowledge of FDA, EMA, ICH, and GCP requirements.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
Save
Mark Applied
Hide
Clinical Research Supervisor
Springdale, Arkansas, United States
OnsiteFull Time
4+ YOEManage research staff and operations in an oncology clinical trials program; 4+ years related experience preferred, bachelor’s or nursing background preferred, CCRP after 2 years, EMR/EDC proficiency.
EMR, Electronic Data Capture (EDC)
1w
Save
Mark Applied
Hide
Sr. Clinical Research Associate
Sparks or Arkansas or California or Colorado or Connecticut or Delaware or Florida or Idaho or Illinois or Indiana or Iowa or Wyoming or Kansas or Kentucky or Montana or Louisiana or Maine or Maryland or Massachusetts or Michigan or Minnesota or Mississippi or Missouri or Nebraska or Nevada or Ohio or Oklahoma or Oregon or Pennsylvania or Tennessee or Texas or Utah or Vermont or Virginia or Washington or Alabama or Arizona
RemoteFull Time
3+ YOEBachelor's degree in healthcare or science, 3 years of field-based CRA experience, clinical trial operations knowledge, and familiarity with GCP, FDA, ISO, HIPAA, and clinical research systems.
Veeva Vault CTMS, Veeva Vault CDMS, Veeva Vault, CTMS, CDMS, FDA CFR, ISO, HIPAA, IRB, EC, CROs, ALCOA
3w
Save
Mark Applied
Hide
Clinical Research Site Director
Little Rock, Arkansas, United States
OnsiteFull Time
5+ YOE5+ years coordinating industry-sponsored clinical trials, site leadership experience, patient-facing clinical skills (consent, assessments, blood draws, medication administration, ECG), regulatory compliance and strong attention to detail.