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Regeneron

Temporary Manager – Clinical Drug Supply & Logistics

Regeneron

. Forecast Investigational Product (IP) supply requirements for multiple clinical trials .

Posted 9/18/2026full-timeUnited StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical supply management, including forecasting, inventory strategy, and vendor management, while ensuring compliance with regulatory standards. Proven ability to lead cross-functional teams and mentor junior staff in the biotechnology and pharmaceutical sectors.

Highest-signal resume keywords
Clinical Supply ManagementForecasting Investigational Product SupplyInteractive Response Technologies (IRT)Regulatory ComplianceVendor Management

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Supply PlanningInventory StrategyResupply ActivitiesIP Distribution ProcessesBudget ManagementProcess InitiativesMetrics TrackingStudy Document ReviewSpecifications DevelopmentTraining Coordination
Soft Skills
LeadershipCommunicationMentoringProblem-SolvingCollaboration
Tools & Technologies
IVRSIWRS
Certifications & Qualifications
MastersMBAPharmD
Industry Keywords
BiotechnologyPharmaceuticalClinical TrialsRegulatory AuthoritiesCROs

About the role

Key responsibilities & impact
  • Forecast Investigational Product (IP) supply requirements for multiple clinical trials
  • Manage IP distribution processes for one or more clinical trials
  • Lead drug supply management and demand forecasting according to IOPS requirements
  • Manage supply planning, timelines, inventory strategy, resupply activities, shipments, returns and destruction
  • Develop and oversee expiry, ancillary and comparator supply strategies
  • Develop specifications and support user testing of IVRS/IWRS systems
  • Monitor clinical supply activities from study start-up through study closure
  • Review and approve IP-related study documents, tools, kit lists and specifications
  • Represent Clinical Drug Supply & Logistics on cross-functional study teams
  • Coordinate training and communicate with CROs, vendors, investigator sites and study teams
  • Act as point of escalation for IP-related and vendor-related issues
  • Provide input into budgets, statements of work, contracts and timelines
  • Create RFPs, review quotes and manage distribution vendor budgets
  • Lead management of IP service vendors and oversee performance, quality, timelines, deliverables and costs
  • Develop and implement process initiatives
  • Track and report supply metrics and supply status to study teams and senior management
  • Mentor or coach junior Clinical Drug Supply & Logistics staff; does not supervise staff

Requirements

What you’ll need
  • At least 5 years of relevant experience in the biotechnology/pharmaceutical industry
  • Minimum 3 years in clinical supply management
  • Masters/MBA/PharmD with 3+ years of relevant industry experience
  • Working knowledge and experience with Interactive Response Technologies (IRT), such as IVRS and IWRS
  • May require 25% travel
  • Ability to work in compliance with Regulatory Authorities’ regulations/guidelines and Regeneron SOPs/WPDs

Benefits

Comp & perks
  • Annual bonuses or other incentive plans
  • Equity awards
  • Pension or retirement benefits
  • 401(k) company match
  • Health and wellness programs
  • Fitness centers
  • Medical, dental, vision, life and disability insurance benefits
  • Paid time off
  • Family support benefits
  • Reasonable accommodation during the recruitment process where required