Role Summary:

The Sr/Exec Director, Clinical Medical Experts provides support to shape and build grp of clinical medical experts in medical affairs..  The Sr/Exec Director, Clinical Medical is accountable for being a highly engaged and productive member a small group of NASH disease experts with strong clinical and applied industry experience to serve as internal experts for the entire organization.  Importantly, the Sr/Exec Director, Clinical Medical is accountable for the integration into and support of the rest of medical affairs – field and headquarters, US and rest of world – and with other functions in Madrigal to include clinical development, regulatory affairs, marketing and market access.  The Sr/Exec Director, Clinical Medical will manage the inevitable competing priorities they will confront as a member of clinical NASH experts (hepatologists/gastroenterologists) to ensure the group is doing the highest value work to support Madrigal’s strategies.

 

Primary Activities:

Organizational Scientific and Clinical Expertise Support:

Communicates scientific information in a balanced and highly credible manner  to external stakeholders

Contribute insights to the global medical affairs leadership team and the cross-functional

Commercial/Medical leadership team regarding clinical, health outcomes and real world evidence gaps

Actively participate in internal or external trade, professional organizations, academic or regulatory working teams on matters that impact field medical affairs operations

 

Medical Affairs Research:

Actively participate in  the Investigator Initiated Research program at Madrigal

Actively participate in the Managed Access or Early Access Program at Madrigal

Actively participate in the Registry program at Madrigal in conjunction with HEOR and Clinical Development

Actively work with HEOR on other real-world data generation projects

Medical Affairs Operational Areas:

Provide support to Medical Information team on development of Standard Response Documents

Provide review support for all medical content review and finalization

Skill Requirements:

Minimum:

Physician (MD/DO or equivalent) with strong liver clinical experience, including NASH

Hepatologist or gastroenterologist preferred with significant liver and NASH experience

Pharma experience preferred – medical affairs and/or clinical development

Significant knowledge of NASH – disease, patient identification, current thought leaders, guidelines and practice patterns

Track record of developing excellent personnel and teams

Excellent interpersonal and communication (written and oral), analytical, and results oriented project management skills

Drug regulatory experience helpful but not required

Possess a thorough understanding of all US compliance guidelines relevant to the pharmaceutical industry and field medical roles

Highly ethical and with strong compliance record

Ability to manage others through change, demonstrating poise under pressure and motivational leadership