Support disease state education and reinforce the importance of diagnostic testing and treatment in cholestatic liver disease, SLOS, BASDs, ZSDs, and CTX per request (e.g. grand rounds, executive presentations and KOL engagements)
Educate physicians utilizing the company’s sponsored testing programs about best practices in interpretation of genetic results
Expertly articulate relevant scientific and clinical information relative to the therapeutic area to HCPs and researchers
Utilize scientific resources to deliver impactful presentations to varying audiences and in a variety of different settings including (but not limited to) advisory boards, patient advocacy groups, and payors
Collaborating with external scientists and clinicians on projects related to the identification and treatment of diseases of interest
Serving as point-of-contact for the sponsored-testing program in cholestasis and lead projects related to its optimization such as transition to WES as well as need for ongoing revisions and reflex testing
Developing and executing strategy that facilitates the reclassification of variants of unknown significance in PFIC
Supporting the development, analyses and dissemination of data from real-world registries and data repositories of genetic causes of cholestasis
Facilitate and advance externally supported research concepts to Vice President of Scientific Affairs
Contributing to the overall strategic plan and developing data generation and dissemination activities that support the plan
Leading the development of scientific publications that support the overall (Livmarli) Brand Plan and Medical Strategic Plan that are directed towards the diagnosis and management of genetic cholestasis along with SLOS, BASDs, ZSDs and CTX
Partnering with other functional teams to develop educational materials for different stakeholders (e.g., physicians, patients) that aid in the diagnosis and management of genetic cholestasis
Educating appropriate internal teams on genetics of cholestasis
Requirements
Masters degree in science such as MPH, MHS, or MS
Minimum of 5 years of experience in medical affairs or clinical or scientific research, and publications
Experience as genetics counselor and/or MSL preferred
Ability to work collaboratively with external stakeholders and internal cross-functional team
Experience developing scientific publications, including liaising with authors and internal stakeholders, adhering to timelines, articulating key objectives of publications, and aligning scientific content to strategic imperatives
Experience with clinical research including experience generating and analyzing data
Proven ability to write and edit content for scientific abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives