Global Regulatory Affairs Scholar

Johnson & Johnson

. Complete a two-year experiential fellowship with advanced, hands-on professional development .

Posted 10/23/2026full-timeUnited StatesMid-LevelSenior💰 $92,000 - $148,350 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates a strong understanding of the global drug development lifecycle and regulatory requirements, with the ability to engage health authorities effectively. Exhibits leadership capabilities and creative problem-solving skills while collaborating across diverse teams.

Highest-signal resume keywords

Bachelor's DegreePhD/PharmD PursuitFDA Regulations KnowledgeLeadership CapabilitiesPharmaceutical Drug Development Understanding

ATS Keywords

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Applicant Tracking System Keywords

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Soft Skills

CollaborationProblem-SolvingPresentation SkillsSelf-MotivatedCuriosity

Industry Keywords

Regulatory AffairsDrug Development LifecycleProduct LabelingPolicy and IntelligenceChemistry Manufacturing and ControlsHealth Authorities EngagementInternational Healthcare SystemsInnovative IdeasStakeholder InfluenceCross-Functional Exposure

About the role

Key responsibilities & impact

Complete a two-year experiential fellowship with advanced, hands-on professional development
Participate in multiple rotations across disease-therapeutic areas and regulatory functions, including Product Labeling, Policy and Intelligence, and Chemistry, Manufacturing and Controls
Develop understanding of the global drug development lifecycle and strategies for engaging health authorities
Learn laws, guidance, and regulatory requirements for drugs and combination products
Tackle real-world projects that build leadership presence and stakeholder influence
Strengthen collaboration, problem-solving, and presentation skills
Build professional networks and cross-functional exposure with different teams
Participate in internal and external meetings
Own a complex capstone project and present results to GRA senior leaders and internal partners

Requirements

What you’ll need

Earned a bachelor's degree (B.S. or B.A.) from a 4-year university program, and/or currently pursuing an advanced degree (PhD/PharmD) in a scientific, technology or engineering-related field from an accredited academic institution, with planned graduation by May 2027
Candidates with early professional experience seeking to develop careers in regulatory affairs
Strong academic track record required
Fundamental understanding of pharmaceutical drug development preferred
Knowledge of current FDA regulations, guidelines, and submission requirements desired
Leadership capabilities in an organizational setting preferred
Ability to work independently and as part of a group
Curiosity and flexibility
Self-motivated with a “can do” approach
Courage to speak your voice and suggest innovative ideas
Creative problem-solving ability
Interest in international healthcare systems and technology contexts

Benefits

Comp & perks

One-way US relocation assistance
Consolidated retirement plan (pension)
Savings plan (401(k))
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year (with specified higher allowances for Colorado and Washington employees)
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Inclusive accommodation support during the interview process