Director, Global Publications Lead

Director, Global Publications Lead

Why Join Intellia?

Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. 

Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done. 

We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.   

How you will Achieve More with Intellia:

The Global Publications Lead will lead the development and oversight of Global Publication plans for Medical Affairs by ensuring that clinical and HEOR data is published according to company SOPs and policies. The Publication Lead is responsible to ensure that information gaps are addressed with strategic publication plans and drive the development of publications to communicate scientific and clinical information for both internal and external stakeholders and customers.

Within this role, you will:

• Strategically develop, lead and complete Publication Plans for assigned programs/therapeutic areas, ensuring robust strategic planning, tactical planning and implementation of congress presentations and manuscript execution in alignment with global publications objectives and initiatives
• Maintain and execute Publication Plans for clinical and HEOR publications for assigned programs/therapeutic in collaboration with a Publications Working Group (PWG) ensuring high quality and timely achievement of landmarks and deliverables
• Drive and coordinate vendor selection and handle vendor medical writing (MW) activities
• Ensure fair balance and integrity of available scientific data of all abstracts, posters, manuscripts and oral presentations
• Build effective partnerships with all stakeholders, including supported programs’ Medical Program Leads, R&D Program Leads, HEOR Program Leads, Statistical Program Leads, IP, and Legal
• Lead the Publication Working Group (PWG) meetings for assigned programs and ensure the timely, accurate execution of all PWG results and action items
• Coordinate/manage writing activities of external agencies and/or internal medical writers
• Critically review/edit sophisticated publication documents for quality, compliance and scientific integrity
• Lead monthly budget management and forecasting of publications spend within Medical Product Plans
• Deliver innovative publication solutions and publication extenders, as appropriate
• Ensure compliance with regulatory requirements as well as industry guidelines and Intellia policies

About You:

Minimum Requirements:

• PharmD, healthcare-related PhD, or MS with significant industry or related medical information experience preferred

• Minimum of 5-7+ years of experience in medical writing, medical publications, and/or communications
• Certification as a Medical Publication Professional (CMPP) is highly desirable
• Willingness to travel (role anticipated to have about ~25% travel component)

Skills:

• Familiarity with publication management tools and systems (i.e. Datavision)
• Critical thinking with an innovative mindset required
• Tight-knit collaboration and stakeholder management, communication and presentation skills
• Tried project management, vendor management, and budget leadership skills are required
• Self-starter with the ability to work collaboratively and the desire to work on a cross functional team
• Experience in development of abstracts, posters, manuscripts is required, ability to perform a literature evaluation is preferred
• Proficient in Microsoft Word, PowerPoint, Excel, and technologically savvy

Meet your future team:

The Medical Affairs Team at Intellia is here because we believe genome editing has incredible potential to treat and cure life-threatening and fatal diseases, and we believe the Intellia has the right people, strategy, and culture to do it well.  Our team is made up of functions related to Medical Program Leadership, Scientific Communications, Patient Advocacy, Governance, Medical Strategy, and External Medical Engagement.

The team is led by our Global Head of Medical Affairs, a physician with over 25 years of experience in large pharma and biotech environments globally. 

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Covid-19 Vaccination Policy: All Intellia employees, regardless of work location, are expected to follow all applicable federal, state, and local public health regulations and guidelines, and are strongly encouraged to follow all public health recommendations, including being vaccinated for COVID-19.

EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.