6 cro manager jobs at 4 companies in Windsor, CO
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Senior Clinical Trial Manager
Seattle or Louisville
$125k-$175k/yr HybridFull Time
6+ YOE1+ MgmtBachelor’s degree or equivalent in Life Sciences and 6–8+ years of pharmaceutical clinical operations experience, including sponsor-side trial management; requires GCP/ICH knowledge, CRO oversight, and team leadership.
Case Report Forms (CRF)
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Senior Digital Product Owner - Lead & Analytics
Chicago or Peoria or Westminster or Irving or Arizona
$113k-$183k/yr OnsiteFull Time
Digital product ownership experience with analytics, lead management, web tagging, attribution, CRO, A/B testing, CRM, and cross-functional collaboration; Python, Snowflake, and SQL preferred.
Adobe Analytics, Google Analytics, Tag Management Systems, Python, Snowflake, SQL, CRM, CMS, PIM, A/B testing
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Senior Digital Product Owner - Lead & Analytics
Broomfield or Chicago or Phoenix
$113k-$183k/yr OnsiteFull Time
Bachelor's degree preferred in computer science, engineering, marketing, business, or related field; product ownership experience, analytics, lead management, web analytics, CRO, A/B testing, CRM, and cross-functional collaboration required.
Adobe Analytics, Google Analytics, Tag Management Systems, Python, Snowflake, SQL, CRM, CMS, PIM, A/B testing
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Associate Director, Clinical Operations
Waltham or Boulder
$185k-$215k/yr HybridFull Time
6+ YOE6+ years clinical development experience, BS/BA preferred, experience leading multi‑phase trials, CRO/vendor management, GCP/ICH/FDA knowledge, SOP development, and ability to travel ~25%.
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Director, Medicinal Chemistry
Louisville, Colorado, United States
$164k-$257k/yr OnsiteFull Time
8+ YOEPhD/MS/BS in chemistry with substantial small-molecule drug discovery experience (PhD 8+ yrs, MS 10+ yrs, BS 12+ yrs). Experience with molecular glue programs, SAR, CRO management, and leadership.
LiveDesign, MOE, Maestro
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Director, Pharmacovigilance
Seattle or Louisville or United States
$204k-$305k/yr HybridFull Time
10+ YOEAdvanced degree or health-related credential plus 10+ years PV experience in biotech/pharma; expertise in global safety regulations, safety databases (Argus, ArisGlobal), vendor/CRO management, aggregate reporting, signal detection, and inspection readiness.
Argus, ArisGlobal