Global Regulatory Affairs Scholar

Johnson & Johnson

. Develop a broad understanding of the global drug development lifecycle and strategies for engaging health authorities .

Posted 10/23/2026full-timeUnited StatesMid-LevelSenior💰 $76,000 - $121,900 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, collaboration, and problem-solving skills while managing complex projects in a cross-functional environment.

Highest-signal resume keywords

Bachelor's DegreeAdvanced Degree In Scientific FieldKnowledge Of FDA RegulationsLeadership CapabilitiesPharmaceutical Drug Development Understanding

ATS Keywords

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Applicant Tracking System Keywords

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Soft Skills

Creative Problem-SolvingCuriosityFlexibilitySelf-MotivationStakeholder Influence

Industry Keywords

Drug Development LifecycleRegulatory AffairsProduct LabelingPolicy And IntelligenceChemistry Manufacturing And ControlsHealthcare SystemsSubmission Requirements

About the role

Key responsibilities & impact

Develop a broad understanding of the global drug development lifecycle and strategies for engaging health authorities
Learn laws, guidance, and regulatory requirements for drugs and combination products while aligning with organizational goals
Complete real-world projects that develop leadership presence, stakeholder influence, 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
Complete multiple rotations across disease-therapeutic areas and regulatory functions, including Product Labeling, Policy and Intelligence, and Chemistry, Manufacturing and Controls

Requirements

What you’ll need

Earned a bachelor's degree (B.S. or B.A.) from a 4-year university program
Earned or is currently pursuing an advanced degree (Master’s level) in a scientific, technology or engineering related field from an accredited academic institution, with planned graduation by May 2027
Early professional experience suited to candidates developing careers in regulatory affairs
Strong academic track record
Fundamental understanding of pharmaceutical drug development preferred
Knowledge of current FDA regulations, guidelines, and submission requirements preferred
Leadership capabilities in an organizational setting preferred
Ability to work independently and as part of a group
Curiosity and flexibility
Self-motivation and a “can do” approach
Courage to speak your voice and suggest innovative ideas
Creative problem-solving ability
Interest in the international context of 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; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
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 the 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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year