3 trial manager jobs at 3 companies in Hawaii

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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
Syneos Health
Syneos Health: Clinical trial and commercialization services for biopharmaceutical firms.
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
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Personal Injury Legal Assistant
Honolulu, Hawaii, United States
OnsiteFull Time
Shaheen & Gordon
Shaheen & Gordon: A full-service law firm providing personalized legal representation and community-focused service.
1+ year legal assistant experience supporting personal injury trial attorneys; managing files, medical records, discovery, court filings, and client communications. Strong administrative, proofreading, and multitasking skills required.
Microsoft Office, Microsoft Outlook, Microsoft Excel, Adobe, Filevine
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Director, Biostatistics
Cambridge or United States or Alaska or Arizona or Hawaii or Michigan or Tennessee
$221k-$249k/yr RemoteFull Time
Amylyx Pharmaceuticals
Amylyx PharmaceuticalsNASDAQ: AMLX: Develops treatments for neurodegenerative diseases and endocrine conditions.
10+ YOEPhD (10+ years) or MSc (14+ years) in statistics/biostatistics/math; proficiency with SAS or R and CDISC; experience designing late-phase clinical trials, regulatory interactions, leadership and communication skills.
SAS, R, CDISC