Responsibilities

• Support the development and execution of public relations plans: Assist in bringing strategic ideas to life by contributing to PR programs that align with client goals and reflect key industry trends.
• Help translate scientific and regulatory milestones: Lead development of internal and external communication materials for data milestones and regulatory approvals that resonate with audiences, including media, healthcare professionals, and patient communities.
• Support high-visibility communications campaigns: Support content creation, media materials, and sponsored content and more as part of high-visibility celebrity and influencer campaigns, with close attention to accuracy, consistency, and brand alignment.
• Lead media material development and monitoring: Collaborate with earned specialists to research media targets, develop media lists, draft outreach materials. Lead team monitoring efforts on a daily basis and around data milestones.
• Collaborate with integrated teams: Partner with colleagues across digital, paid, media, and analytics functions to support the development of integrated campaign elements.
• Ensure smooth project management: Manage project timelines and team bandwidth, making sure execution stays on track amid tight turns.
• Pitch in where needed: Be ready to support teammates with coordination, documentation, and execution across various projects and deliverables.
• Serve as a junior team mentor: Provide direction and feedback to junior team members in daily and ongoing responsibilities; mentoring them for growth within the team. Participate in the hiring and onboarding of new team members.

Requirements

• 4+ years of PR/communications experience, PR agency experience will be advantageous
• High science expertise is a must, along with a strong commitment to learning and applying data-driven insights
• S Thorough understanding of rules and regulations in consumer and / or pharma healthcare space; experience in oncology and supporting FDA approvals, medical meetings and data readouts is a strong plus
• Experience with Veeva and preparing documents for MLR reviews is a strong advantage.
• Balanced organized workstyle allowing for equal success whether stepping up and driving work independently or collaborating and project managing with the team
• Sureness in all the skills one would expect at this level including understanding the regulatory environment; engaging directly with clients on most agendas; project management; writing; content development; presenting; digital; social; budget; preference for working as part of a highly collaborative team

Preferred

• Experience in oncology and supporting FDA approvals, medical meetings and data readouts is a strong plus
• PR agency experience will be advantageous
• Experience with data-driven insights and healthcare regulatory environments is preferred

Benefits

• Medical & Prescription
• Dental
• Vision
• Flexible Spending Accounts
• 401k (with discretionary employer match)
• Employee Stock Purchase Plan
• Short-Term Disability, Long-Term Disability & Life Insurance
• Vacation, Sick & Personal Days
• 14.5 Paid Company Holidays
• Parental Leave