Assistant Director, Medical Evidence Generation

Ionis•Carlsbad, CA

9d•$140,000 - $160,000•Hybrid

About The Position

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals. At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees. With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive. We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career! ASSISTANT DIRECTOR, MEDICAL EVIDENCE GENERATION SUMMARY: The Assistant Director of Medical Evidence Generation (MEG) will be responsible for supporting Ionis’ medical evidence generation strategy within the cardiometabolic and specialty/rare therapeutic areas. This role will involve working closely with the MEG TA leads as well as cross-functional teams including Medical Affairs, Clinical Development, HEOR, and Commercial teams to support the design and conduct of observational research studies. This role will report to the Director of Medical Evidence Generation.

Requirements

A PhD or Master’s degree in pharmacoepidemiology, epidemiology, biostatistics, public health, or related field with at least 4 years of experience (PhD level) or 6 years of experience (Master’s level) in Evidence Generation in the pharmaceutical industry.
Experience designing and leading observational research studies, including the use of real-world data.
Organized with exceptional project management skills
Strong knowledge of observational and Phase 4 study design and implementation.
Survey research and PRO experience.
Strong analytical and problem-solving skills.
Experienced with publishing their research.
Excellent verbal and written communication and presentation skills.
Ability to work collaboratively with cross-functional teams.
Strong leadership skills, including experience leading cross-functional teams.
Ability to work independently and manage multiple projects simultaneously.

Nice To Haves

Experience with data analysis, including programming in R and/or SAS, preferred.

Responsibilities

Support the design and conduct of Phase 4 study designs, including observational studies, and collaborative studies with academic institutions, patient advocacy groups, or other external organizations to generate additional medical evidence for marketed products.
Conduct literature reviews.
Collaborate with cross-functional teams including Medical Affairs, Clinical Development, HEOR, and Commercial teams to ensure that medical evidence generation activities are aligned with the overall business objectives.
Develop and review study protocols, statistical analysis plans, table shells, case report forms, and patient/caregiver surveys as part of study implementation.
Manage projects, including formulating agendas and meeting minutes for study meetings, vendor management, and management of study timelines.
Present medical evidence to internal and external stakeholders, including at scientific conferences, and other relevant forums.