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Philips

Senior Manager, Scientific Communications

Philips

. Lead global scientific communication strategy aligned with organizational objectives, product strategy, and industry standards .

Posted 10/6/2026full-timeRemote • United StatesSenior💰 $133,000 - $237,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading scientific communication strategies and developing compliant scientific content, with a strong focus on stakeholder management and publication planning within the medical device or biotech industry.

Highest-signal resume keywords
Medical Affairs ExpertiseRegulatory Requirements KnowledgePublication Planning and ExecutionStakeholder ManagementTechnical Presentations

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Scientific Content DevelopmentClinical Study ReportsManuscript AuthoringAbstract DevelopmentData Integrity MaintenanceEvidence CaptureRegulatory Dossier PreparationCommunications DevelopmentScientific Literature ReviewsProject Tracking
Soft Skills
Coaching Junior Team MembersCross-Functional CollaborationInfluencing StakeholdersCommunication SkillsTeam Performance Advancement
Tools & Technologies
Publication TemplatesManuscript SoftwareEvidence-Management ResourcesSubmission WorkflowsSOP RepositoriesVirtual Collaboration Platforms
Industry Keywords
Medical Device IndustryBiotech IndustryClinical AffairsTherapeutic Area KnowledgeCommercial Acumen

About the role

Key responsibilities & impact
  • Lead global scientific communication strategy aligned with organizational objectives, product strategy, and industry standards
  • Develop and refine manuscripts, abstracts, conference presentations, clinical study reports, briefing documents, regulatory dossiers, and other compliant scientific and regulatory content
  • Oversee submission, review, approval, and publication workflows
  • Maintain SOPs for evidence capture, device and system performance, safety, and data integrity
  • Implement best practices to improve communication quality, efficiency, timeliness, and impact
  • Partner with senior leadership, cross-functional teams, internal stakeholders, external authors, investigators, speakers, and scientific organizations
  • Align messaging and support collaborative research
  • Manage strategic relationships and deliver scientific training
  • Coach junior team members and advance team performance
  • Strengthen the organization’s scientific credibility, visibility, and influence through accurate, clear, ethical, and timely communications
  • Use publication and regulatory document templates, manuscript and presentation software, literature and evidence-management resources, submission and review workflows, SOP repositories, project-tracking tools, and virtual collaboration platforms to develop, approve, track, and disseminate scientific materials
  • Travel up to 25%

Requirements

What you’ll need
  • Minimum 5 years of experience with a Bachelor’s degree or 3 years of experience with a master’s degree in Medical or Clinical Affairs within the medical device or biotech industry, or an equivalent field
  • Experience with similar therapeutic area medical device products strongly preferred
  • Bachelor’s or master’s degree in medical science, Nursing, or an equivalent field
  • MD or PhD in Nursing, Medical Science, or an equivalent discipline strongly preferred
  • No specific certification is required or preferred
  • Commercial and business acumen
  • Clinical and Medical Affairs expertise
  • Knowledge of regulatory requirements
  • Stakeholder management
  • Publication planning and execution
  • Technical presentations
  • Communications development
  • Scientific literature reviews
  • Content authoring tools
  • Ability to perform minimum physical, cognitive, and environmental job requirements with or without accommodation
  • 5–7 years of Medical or Clinical Affairs experience in the medical device or biotech industry preferred
  • Ability to communicate technical and scientific information effectively while influencing cross-functional stakeholders
  • Willingness and ability to travel up to 25%
  • US work authorization required; candidates requiring current or future visa sponsorship will not be considered
  • Must reside in or within commuting distance to posted locations

Benefits

Comp & perks
  • Annual incentive bonus may be offered
  • Sales commission may be offered
  • Long-term incentives may be offered
  • Generous PTO
  • 401k with up to 7% match
  • HSA with company contribution
  • Stock purchase plan
  • Education reimbursement
  • Comprehensive Philips Total Rewards benefits program