
Content Lead
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in United States.
• Conduct thorough copyediting and proofreading of DTC web assets.
• Ensure user-friendly flows, accessible consumer messaging, impeccable grammar, and adherence to brand guidelines.
• Oversee and manage comprehensive content workflows and timelines.
• Handle digital copy submissions, tactic routing, and approval processes in Veeva Vault or similar platforms.
• Participate in and lead live MLR review sessions, documenting feedback and annotations in real time.
• Collaborate with designers and content creators to implement regulatory and consumer-focused updates.
• Record and uphold operational guidelines based on feedback from reviewers.
• Support content verification during UAT to ensure that deployments align with MLR-approved copy, disclaimers, and ISI elements.
• Assess handoffs and tool utilization to enhance content operations and reduce submission turnaround time.
• Bachelor’s degree in English, Journalism, Communications, Marketing, Healthcare Communications, or a related field.
• Over 10 years of professional experience in digital content strategy, copyediting, or content operations, with a solid background in DTC digital properties within the pharmaceutical, biotech, or healthcare industries.
• Proven experience in developing and refining web content to enhance consumer/patient health literacy and engagement.
• Proficiency in line-editing, copyediting, proofreading, and technical grammar verification for consumer-facing digital platforms.
• Significant hands-on experience managing digital content via Veeva Vault Promomats or comparable MLR review software like Zinc or Pepper.
• Experience in facilitating and managing live MLR/PMRC review sessions and converting regulatory feedback into actionable revisions.
• Excellent verbal and written communication skills in English.
• Advanced understanding of English grammar, syntax, punctuation, mechanics, and style guidelines.
• Proven expertise in using Veeva Vault for regulatory submission and tracking purposes.
• Strong understanding of pharmaceutical claims, Fair Balance, and the placement of Important Safety Information (ISI) on web platforms.
• Exceptional attention to detail in formatting, structural alignment, and consumer readability.
• Competitive benefits package.
• Ongoing training opportunities.
• Personal and professional development prospects.
• Flexible remote work environment.
• Standard business hours from Monday to Friday.
• No travel required.
Directive
Navitus Health Solutions
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