Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Philips

Senior Manager, Scientific Communications

Philips

. Lead global scientific communication strategy and execution for Ambulatory Monitoring & Diagnostics .

Posted 10/7/2026full-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 scientific communication strategy and execution, with a strong focus on publication planning, regulatory compliance, and stakeholder management within the medical device or biotech industry. Proven ability to develop high-quality scientific content and manage cross-functional collaborations effectively.

Highest-signal resume keywords
Scientific Communication StrategyPublication Planning and ExecutionRegulatory Requirements KnowledgeStakeholder ManagementClinical and Medical Affairs Expertise

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Content Authoring ToolsTechnical PresentationsScientific Literature ReviewsClinical Study ReportsRegulatory DossiersManuscript DevelopmentAbstract DevelopmentConference PresentationsEvidence CaptureData Integrity
Soft Skills
CollaborationCoachingCommunication DevelopmentStrategic Relationship ManagementLeadership
Tools & Technologies
Publication TemplatesProject-Tracking ToolsSOP RepositoriesVirtual Collaboration PlatformsEvidence-Management Resources
Industry Keywords
Medical DeviceBiotechClinical AffairsMedical ScienceTherapeutic Area Expertise

About the role

Key responsibilities & impact
  • Lead global scientific communication strategy and execution for Ambulatory Monitoring & Diagnostics
  • 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, support collaborative research, manage strategic relationships, deliver scientific training, and coach junior team members
  • Strengthen the organization’s scientific credibility, visibility, and influence
  • 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
  • Deliver compliant publication and regulatory deliverables, timely research dissemination, effective conference engagement, stakeholder alignment, evidence currency, and individual and team goals

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
  • 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
  • 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
  • No specific certification is required or preferred

Benefits

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