Responsibilities:

• Assist in creation of integrated scientific communication strategy and tactical publication plans for therapeutic areas in accordance with brand and medical strategies and incorporating modern digital channels and tools
• Lead execution of tactical publication plans which entails publications development in timely, compliant manner following Ardelyx publications policy, ICMJE, and GPP guidelines
• Partner effectively with internal and external authors, other internal stakeholders and medical communication agencies to complete publication milestones
• Lead development of other audience (APPs, RDs, non-expert physicians, PCPs, patient advocacy outreach) tailored publication extenders including but not limited to infographics, plain language summaries, visual abstract, short audio/videos, and podcasts
• Co-lead annual publication planning and quarterly publication team meetings
• Maintain publication metrics and keep up with evolving metrics measure, serve as the point person with relevant medical affairs analytics partners
• Lead planning, coverage and reporting of major and smaller specialty GI and Nephrology congresses. Provide on-site support for Tier-1 conferences
• Lead weekly literature surveillance, discussion forums, develop and distribute literature reports
• Ensure alignment of the publications plan with all corporate policies and industry guidelines (ICMJE, GPP3)
• Manage relationships with medical communications agencies

Qualifications:

• Advanced degree in Life Sciences: PhD (preferred), PharmD, or MD with 5+ years of experience in scientific publications within Pharma/Biotech industry or medical communication agency or equivalent experience
• In depth knowledge of ICMJE and GPP guidelines, proficiency in industry supported publications development process, CMPP certification preferred
• Strong understanding of clinical trial conduct, real-world data generation and other data sources for publications such as SLRs, expert opinion articles
• Ability to quickly and consistently build and maintain high level of trust and effectively collaborate with internal and external stakeholders
• Demonstrated experience executing projects with competing priorities and tight deadlines
• Strong ability to interpret, organize and communicate complex scientific data in a concise manner; ability to generate insights
• Strong sense of urgency, project planning and management skills
• Knowledge of pharmaceutical and promotional compliance guidelines, laws, industry standard practice, and applicable regulatory guidelines pertaining to medical content development
• Demonstrated customer-centered approach
• Up to 10% travel, including overnight and occasional weekend travel
• Attendance at periodic national internal and external meetings and medical congresses

Ardelyx is an equal opportunity employer.

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