Apellis

The Associate Director, Ophthalmology is a key member of the Global Medical Affairs team who will work closely with medical affairs and cross-functional stakeholders to implement key aspects of the Global Medical strategy for ophthalmology and potential global launches of pegcetacoplan in geographic atrophy (GA) secondary to age-related macular degeneration (AMD).. Work closely with the Biostatistics department to support the analysis of clinical data across multiple pegcetacoplan ophthalmology studies. Develop novel approaches to data visualization in support of evidence generation efforts. Drive and/or assist in development and implementation of evidence generation strategy (Phase IV, real-world evidence/HEOR, post hoc analyses, investigator initiated trials and collaborative research),. Significant experience across drug development stages, particularly in late-stage development, launch, and post approval setting

associate director medical affairs

Job Description Job Description Position Summary:
The Associate Director, Ophthalmology is a key member of the Global Medical Affairs team who will work closely with medical affairs and cross-functional stakeholders to implement key aspects of the Global Medical strategy for ophthalmology and potential global launches of pegcetacoplan in geographic atrophy (GA) secondary to age-related macular degeneration (AMD). These activities may include data generation, insight gathering, and scientific communications/publications, as the medical affairs team prepares for launch readiness in the ophthalmology space.
Key Responsibilities Include:
Support the development of tactics on the Global Evidence Generation team in alignment with product strategy
Work closely with the Biostatistics department to support the analysis of clinical data across multiple pegcetacoplan ophthalmology studies
Develop novel approaches to data visualization in support of evidence generation efforts
Provide data analysis support to various workstreams
Support the medical communications strategy across multiple clinical studies
Drive and/or assist in development and implementation of evidence generation strategy (Phase IV, real-world evidence/HEOR, post hoc analyses, investigator initiated trials and collaborative research),
Collaborate with cross functional team on approaches to fill identified data and/or communication gaps in alignment with overall strategic objectives
Serve as strategic/scientific resource to cross-functional stakeholders
Education, Registration & Certification:
PhD, Pharm D or MD level degree or equivalent required
Experience:
2-5 years + experience in pharmaceutical/biotechnology medical affairs organization
Experience in retina/ophthalmology therapeutic area strongly preferred
Experience in immunology and ocular inflammation is preferred
Agency management experience preferred
Skills, Knowledge & Abilities:
Significant experience across drug development stages, particularly in late-stage development, launch, and post approval setting
Experience interpreting statistical analyses strongly preferred
Expertise developing different approaches to data analyses strongly preferred
Experience with data visualization tools is a plus
Strong leadership skills, including demonstrated ability to lead a cross-functional team, and influence at all levels of an organization
Excellent oral and written communication skills, including presentation and facilitation
Ability to work independently and with flexibility to handle workflow in a fast-paced environment
Some travel will be required, up to 40%
Benefits and Perks:
Apellis offers a great benefit package which includes: health insurance with full premium coverage, 401K with company match, paid time off (PTO), long- term disability insurance, life insurance and more! Visit https://apellis.com/careers/ to learn more. Company Background:
Apellis Pharmaceuticals, Inc. is a global biopharmaceutical company that combines courageous science and compassion to develop life-changing therapies for some of the most challenging diseases patients face. We ushered in the first new class of complement medicine in 15 years and now have two approved medicines targeting C3. These include the first and only therapy for geographic atrophy, a leading cause of blindness around the world. With nearly a dozen clinical and pre-clinical programs underway, we believe we have only begun to unlock the potential of targeting C3 across many serious diseases.
For more information, please visit http://apellis.com or follow us on Twitter and LinkedIn EEO Statement:
Apellis is an equal opportunity employer and complies with all applicable federal, state and local fair employment practices laws. Apellis strictly prohibits and does not tolerate discrimination against employees, applicants or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including gender nonconformity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, marital status, AIDS/HIV status, smoker/nonsmoker, and occupational pneumoconiosis or any other characteristic protected under applicable federal, state or local law.
For San Francisco postings: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. #J-18808-Ljbffr

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