Senior Manager, Scientific Communications

Job not on LinkedIn

🔥 2 minutes ago

🏈 Alabama, Alaska, +43 more states – Remote

🏈 Alabama – Remote 🐻 Alaska – Remote 🌵 Arizona – Remote 🏄 California – Remote ⛰️ Colorado – Remote 🦌 Connecticut – Remote 🐊 Florida – Remote 🌺 Hawaii – Remote 🥔 Idaho – Remote 🌽 Illinois – Remote 🌾 Iowa – Remote 🌪️ Kansas – Remote 🐎 Kentucky – Remote ⚜️ Louisiana – Remote 🦞 Maine – Remote 🌾 Nebraska – Remote 🎰 Nevada – Remote 🗻 New Hampshire – Remote 🏖️ New Jersey – Remote 🌶️ New Mexico – Remote 🗽 New York – Remote 🌲 North Carolina – Remote 🌾 North Dakota – Remote 🏈 Ohio – Remote 🌪️ Oklahoma – Remote 🌲 Oregon – Remote 🦀 Maryland – Remote 🍂 Massachusetts – Remote 🚗 Michigan – Remote ❄️ Minnesota – Remote 🎸 Mississippi – Remote 🏰 Missouri – Remote 🔔 Pennsylvania – Remote ⚓ Rhode Island – Remote 🌴 South Carolina – Remote 🗿 South Dakota – Remote 🎸 Tennessee – Remote 🤠 Texas – Remote ⛷️ Utah – Remote 🍁 Vermont – Remote ⚔️ Virginia – Remote ☕ Washington – Remote ⛰️ West Virginia – Remote 🧀 Wisconsin – Remote 🦬 Wyoming – Remote

💵 $133k - $237k / year

⏰ Full Time

🟠 Senior

🗣️ Communications

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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Philips

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare • Healthcare Insurance • Biotechnology

Philips is a global health technology company committed to improving people's health and well-being through meaningful innovation. They focus on various domains including personal health, diagnosis and treatment, and connected care, striving to provide advanced technologies and solutions that enhance health outcomes for individuals and healthcare providers alike.

📋 Description

• 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

• 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

• 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