Associate Director, Scientific Communications, Global Immunology Medical Affairs

Johnson & Johnson

. Lead publication planning, development, maintenance, and execution for assigned studies, assets, and therapeutic areas .

Posted 10/12/2026full-timeUnited StatesSenior💰 $137,000 - $235,750 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in scientific communication and publication planning, with a strong ability to lead cross-functional teams and deliver high-quality scientific materials. Proficient in navigating complex projects within the pharmaceutical industry while ensuring compliance with publication standards.

Highest-signal resume keywords

Scientific CommunicationPublication PlanningProject ManagementStakeholder EngagementClinical Data Interpretation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Publication PlanningScientific Communication Materials DevelopmentClinical Data AnalysisEvidence Dissemination PracticesProject ManagementMatrix Organization NavigationScientific Literature ReviewStatistical Analysis UnderstandingTherapeutic Area ExpertiseRegulatory Compliance

Soft Skills

CollaborationInfluencing SkillsOrganizational SkillsMentoringCommunication Skills

Tools & Technologies

AI TechnologiesPublication Management Software

Industry Keywords

Pharmaceutical IndustryBiotechnologyMedical CommunicationsICMJE GuidelinesGPP StandardsCONSORT GuidelinesAMA GuidelinesClinical ResearchReal-World EvidenceCross-Functional Teams

About the role

Key responsibilities & impact

Lead publication planning, development, maintenance, and execution for assigned studies, assets, and therapeutic areas
Lead scientific communication deliverables including manuscripts, abstracts, posters, oral presentations, congress materials, and plain language summaries
Identify data dissemination opportunities that maximize scientific impact and support scientific exchange
Facilitate publication planning discussions with investigators, authors, and internal stakeholders
Monitor publication progress, identify risks, and implement mitigation strategies
Partner with publication managers, medical writers, and external vendors to deliver scientific communications on time and within scope
Serve as a scientific communications subject matter expert for assigned therapeutic areas
Develop expertise in disease states, treatment landscapes, clinical development programs, real-world evidence, and scientific literature
Review, analyze, and interpret clinical and scientific data
Provide scientific leadership and quality oversight for publication materials
Translate complex scientific data into clear, evidence-based communications
Monitor external scientific developments, competitive activities, and standards of care
Ensure communications accurately reflect methodologies, statistical analyses, outcomes, and clinical relevance
Collaborate with Medical Directors, Clinical Development, Biostatistics, Programming, and Medical Affairs stakeholders
Build relationships with investigators, authors, scientific experts, and publication contributors
Ensure compliance with company policies, publication standards, and ICMJE, GPP, CONSORT, and AMA guidelines
Oversee publication vendors and agency partners
Lead cross-functional publication teams and scientific communication initiatives
Mentor publication managers, medical writers, agency partners, and contractors
Provide recommendations to leadership on publication opportunities, communication priorities, and process enhancements
Contribute to departmental initiatives and Scientific Communications capability-building

Requirements

What you’ll need

Bachelor's degree in a scientific, healthcare, or related discipline
5-7 years of relevant experience in Scientific Communications, Medical Affairs, Publications, Clinical Research, Medical Communications, or related pharmaceutical industry functions
Demonstrated experience leading publication planning and execution within pharmaceutical, biotechnology, or medical communications environments
Experience developing and overseeing scientific communication materials, including manuscripts, abstracts, posters, congress presentations, and related deliverables
Experience collaborating with medical writers, publication vendors, investigators, and cross-functional scientific teams
Experience managing multiple complex projects within a matrixed organization
Strong scientific acumen and ability to critically evaluate, interpret, and communicate clinical and scientific data
Strong knowledge of publication planning, scientific communications, and evidence dissemination practices
Thorough understanding of GPP, ICMJE, CONSORT, AMA, and related publication standards
Excellent scientific communication, stakeholder engagement, and collaboration skills
Strong project management, organizational, and prioritization capabilities
Demonstrated ability to influence across functions and navigate a matrixed environment
Proven ability to lead projects, drive execution, and deliver high-quality results
Commitment to scientific excellence, compliance, continuous learning, and operational effectiveness
Commitment to learning and applying emerging technologies such as AI, while building team AI literacy and reinforcing responsible use

Benefits

Comp & perks

Annual performance bonus eligibility
Medical, dental, and vision insurance
Life insurance
Short- and long-term disability insurance
Business accident insurance
Group legal insurance
Pension plan
401(k) savings plan
Long-term incentive program
Vacation: up to 120 hours per calendar year
Sick time: up to 40 hours per calendar year; up to 56 hours for employees residing in Washington State
Holiday pay, including floating holidays: up to 13 days per calendar year
Work, Personal and Family Time: up to 40 hours per calendar year
Hybrid work model with regular onsite collaboration and flexibility to work remotely in accordance with company policy