Added
26 days ago
Type
Full time
Salary
Upgrade to Premium to se...

Related skills

project management regulatory affairs quality control medical affairs veeva

📋 Description

  • Owns the day-to-day administration and execution of designated MLR processes while supporting the
  • Serves as a business administrator for the document management platform (Veeva PromoMats and
  • Serves as primary point of contact for scheduling and facilitating MLR meetings, including
  • Prepares and scribes clear meeting minutes, decision logs and action items; circulates them for
  • Performs quality control on submitted materials, including verification of final documents against
  • Gathers and maintains the forward-looking submission forecast with brand and medical sponsors, and

🎯 Requirements

  • Minimum bachelor’s degree in a life science, communications, or related field
  • Minimum of 5-7 years in pharmaceutical, biotechnology, or medical device, with at least 3 to 4
  • Experience with Veeva or a comparable electronic document and promotional review management system
  • Working knowledge of FDA OPDP expectations for promotional materials, including fair balance
  • Strong written communication — specifically, the ability to prepare meeting minutes, decisions, and
  • Demonstrated ownership of recurring, deadline-driven, cross-functional meetings, with proven

🎁 Benefits

  • Market-leading compensation
  • 401(k) with employer match
  • Employee Stock Purchase Program (ESPP)
  • Pre-tax commuter benefits (transit and parking)
  • Referral bonus for hired candidates
  • Subsidized lunch and parking on in-office days
Get alerts for new remote operations jobs
A weekly email with new matches. Unsubscribe anytime.
Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Operations Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Related Operations Jobs

See more Operations jobs →