Associate Director, Medical & Scientific Affairs

ANI Pharmaceuticals, Inc.

. Support development and manage execution of publication and scientific communication plans across the rare disease portfolio .

Posted 11/6/2026full-timePrinceton • New Jersey • United StatesMid-Level💰 $175,000 - $230,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing scientific publications and communications within the pharmaceutical industry, with a strong focus on rare diseases. Capable of developing high-quality scientific content and navigating regulatory compliance while collaborating effectively across functions.

Highest-signal resume keywords

Advanced Scientific/Clinical Degree5+ Years Experience in Medical AffairsPublication Planning ExpertiseStrong Understanding of Regulatory ComplianceExcellent Written and Verbal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Publication DevelopmentScientific CommunicationClinical Trial Result InterpretationMedical Material Review ProcessesData SynthesisProject ManagementStrategic ThinkingAnalytical ThinkingCross-Functional CollaborationAttention to Detail

Soft Skills

Interpersonal AbilitiesCollaboration SkillsAbility to Thrive in Fast-Paced EnvironmentsIndependent Scientific JudgmentCommitment to Compliance

Industry Keywords

Pharmaceutical IndustryBiotech IndustryRare DiseaseGPP StandardsICMJE RecommendationsMedical AffairsScientific DisseminationEvidence-Based CommunicationExternal Publication AgenciesMedical Communication Agencies

About the role

Key responsibilities & impact

Support development and manage execution of publication and scientific communication plans across the rare disease portfolio
Manage scientific publications, including peer-reviewed manuscripts, abstracts, posters, oral presentations, and plain language summaries
Identify publication opportunities, evidence gaps, and scientific dissemination priorities with cross-functional stakeholders
Coordinate with external investigators, authors, and publication agencies on publication development, review, and submission
Recommend peer-reviewed journals, scientific congresses, and other evidence-dissemination channels
Develop core scientific narratives, medical slide decks, disease-state educational materials, and evidence-based scientific communication resources
Translate clinical trial results, real-world evidence, and emerging scientific data into clear, balanced scientific communications
Coordinate scientific congress activities and related materials
Support scientific review of materials for advisory boards, investigator meetings, and Medical Affairs engagements
Represent Medical Affairs in medical, legal, and regulatory review processes
Manage external publication and medical communication agencies, including timelines, deliverables, and budgets
Independently manage assigned initiatives and coordinate stakeholders to ensure timely, high-quality outputs

Requirements

What you’ll need

Advanced scientific/clinical degree required (PharmD, PhD, MD, or equivalent)
Minimum of 5 years of relevant experience in Medical Affairs, Scientific Communications, Publication Planning, or related functions within the pharmaceutical or biotech industry
Rare disease experience strongly preferred
Strong understanding of pharmaceutical industry regulatory and compliance requirements
Knowledge of medical material review processes and scientific publication standards, including GPP and ICMJE recommendations
Experience managing publication development, medical and scientific communication deliverables, cross-functional review processes, and external publication or medical communication agencies
Experience interpreting and communicating clinical trial results, real-world evidence, and other scientific data to healthcare and scientific audiences
Scientific and clinical expertise with the ability to interpret and communicate complex data
Strategic and analytical thinking
Cross-functional leadership and collaboration
Attention to detail and commitment to compliance
Strong project management skills
Ability to develop high-quality scientific content and deliver impactful medical information services
Demonstrated ability to synthesize complex scientific data into clear, concise, and balanced communications
Excellent written and verbal communication skills; strong interpersonal and collaboration abilities
Ability to thrive in a fast-paced, evolving rare disease environment with a high degree of autonomy and accountability
Ability to exercise independent scientific judgment, manage competing priorities, and provide recommendations to Medical Affairs leadership

Benefits

Comp & perks

Competitive short-term and long-term incentive program based on performance and company results
Health insurance coverage
Life and disability insurance
Retirement savings plans
Paid leave programs
Paid holidays
Paid time off
Many benefits are subsidized or fully paid for by the company