Senior Manager, Scientific Communications

This is a fully remote position, open to applicants in Alabama, +45 more states.

📋 Description

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

• Create and enhance manuscripts, abstracts, conference presentations, clinical study reports, briefing documents, regulatory dossiers, and other compliant scientific and regulatory materials.

• Supervise submission, review, approval, and publication processes.

• Maintain standard operating procedures (SOPs) for evidence capture, device and system performance, safety, and data integrity.

• Implement best practices to enhance communication quality, efficiency, timeliness, and impact.

• Collaborate 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 mentor junior team members.

• Enhance the organization’s scientific credibility, visibility, and influence.

• Utilize 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.

• Ensure the delivery of compliant publication and regulatory outputs, timely research dissemination, effective conference participation, stakeholder alignment, evidence currency, and achievement of individual and team objectives.

⛳️ Requirements

• A minimum of 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 a related field.

• Experience in similar therapeutic area medical device products is highly preferred.

• Bachelor’s or Master’s degree in medical science, Nursing, or a related field.

• An MD or PhD in Nursing, Medical Science, or a comparable discipline is strongly preferred.

• Strong commercial and business acumen.

• Expertise in Clinical and Medical Affairs.

• Familiarity with regulatory requirements.

• Proficiency in stakeholder management.

• Experience in publication planning and execution.

• Skills in technical presentations.

• Development of communications.

• Conducting scientific literature reviews.

• Proficiency with content authoring tools.

• Capability to meet minimum physical, cognitive, and environmental job requirements with or without accommodation.

• Willingness and ability to travel up to 25%.

• US work authorization is required; candidates needing current or future visa sponsorship will not be considered.

• Must live in or be within commuting distance to the specified locations.

• No specific certification is required or preferred.

🏝️ Benefits

• Generous paid time off (PTO).

• 401k plan with up to 7% matching.

• Health Savings Account (HSA) with company contributions.

• Stock purchase plan.

• Education reimbursement.

• Potential annual incentive bonus.

• Possible sales commission or long-term incentives.

• Comprehensive benefits program through Philips Total Rewards.