Senior AD, Scientific Affairs, Medical Information, Medical Review

Boehringer Ingelheim

. Develop, maintain, and continuously improve U.S.

Posted 9/15/2026full-timeRemote • United StatesSenior💰 $165,600 - $294,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced expertise in Medical Information and Medical Review, with a strong focus on compliance, regulatory guidelines, and the clinical development process. Capable of delivering scientifically balanced content and actionable insights while collaborating effectively across various functions.

Highest-signal resume keywords

Advanced Degree Related To HealthcarePharmaceutical Industry ExperienceClinical Knowledge Of Assigned Therapeutic AreasU.S. Medical Information PracticeExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical Information DevelopmentRegulatory ComplianceClinical Data InterpretationMedical Affairs FunctionsPromotional Material ReviewData Integrity VerificationMedical TrainingProject ManagementCustomer Inquiry ResponseProcess Improvement

Soft Skills

Customer FocusInfluencing SkillsCross-Functional CollaborationFlexibilityBusiness Acumen

Industry Keywords

FDA RegulationsPhRMA GuidelinesClinical Practice EnvironmentMedical Review CommitteeTherapeutic AreasSOP ComplianceVendor ManagementContinuous ImprovementMedical CommunicationsStakeholder Engagement

About the role

Key responsibilities & impact

Develop, maintain, and continuously improve U.S. Medical Information assets
Serve as Medical Reviewer on the Human Pharma Review Committee
Support MLR review of U.S. medical and promotional communications
Partner with Medical Affairs Strategy and Global Medical Information to deliver accurate, scientifically balanced, globally aligned content
Plan and prioritize Medical Information response content using customer inquiries, emerging evidence, and external trends
Provide actionable insights for cross-functional medical and business strategies
Advise project owners on material feasibility and provide solution-oriented guidance for HPRC submissions
Develop and review Medical Information content, including FAQs, SSRCs, customized responses, dossiers, and training resources
Collaborate with Global Medical Information, Medical Affairs, Regulatory Affairs, Patient Safety & Pharmacovigilance, and externally facing functions
Maintain documentation of review activities, track changes, and provide stakeholder feedback
Provide medical training and support to contact center and internal stakeholders
Review promotional and non-promotional materials for accuracy, clarity, and compliance
Verify data integrity and interpretation against clinical evidence, product information, disease-state knowledge, regulations, and internal standards
Collaborate with medical affairs strategy, marketing, sales, legal, regulatory affairs, and operations
Maintain comprehensive knowledge of product information, clinical data, medical advancements, regulatory guidelines, and industry best practices
Perform business in accordance with FDA regulations, PhRMA Guidelines, and company policies
Build internal awareness of the Medical Information and Medical Review group
Support vendor training, quality, training, innovation, and department core functions
SAD: Provide leadership and advanced Medical Information and Medical Review expertise
SAD: Drive continuous process and system improvement based on evolving customer needs
May participate in external activities such as DIA and PhactMI

Requirements

What you’ll need

Advanced Degree Related to Healthcare focus (e.g., PharmD, NP/PA, MD, PhD) from an accredited institution
AD: Minimum of two (2) years of experience in a clinical practice environment, including Residency training
AD: Three-plus (3+) years of industry experience, preferably with experience in development and/or medical affairs
AD: At least three to five (3-5) years pharmaceutical industry experience or completion of a two-year Boehringer Fellowship program in MI or equivalent
SAD: Minimum of two (2) years of experience in a clinical practice environment, including Residency training, and three-plus (3+) years of industry experience
SAD: At least seven (7) years pharmaceutical industry experience in MI or equivalent
Clinical knowledge of assigned therapeutic areas
Understanding of the clinical development process, medical affairs functions, product commercialization, pharmaceutical regulations, and regulatory requirements
Knowledge and experience with U.S. Medical Information practice
Experience supervising staff across medical information and third-party vendors
Ability to ensure compliance with SOPs, policies, and work instructions
Demonstrated customer focus, customer satisfaction, and continuous process/asset improvement
Ability to work cross-functionally at franchise and enterprise levels
Flexibility working with internal and external stakeholders
Highly developed ability to influence and work effectively through others
Business acumen and judgment balancing scientific standards with business relevance and impact
Excellent communication skills
Must be legally authorized to work in the United States without restriction
Must be willing to take a drug test and post-offer physical, if required
Must be 18 years of age or older

Benefits

Comp & perks

Competitive compensation and benefit programs
Healthy working environment
Meaningful work
Mobility opportunities
Networking opportunities
Work-life balance
Role-specific variable or performance-based bonus may be available
Other compensation elements may be available