(Sr) Medical Affairs Scientific Director

GRIFOLS, S.A.

1d•Hybrid

About The Position

Support the development of scientifically-sound medical plans in Pulmonology and Critical Care related therapeutic areas. Develop and lead Medical Affairs initiatives and strategies aligned with the global and US medical plan to support innovation and company goals. Provide medical guidance and consultation to internal stakeholders and educate external customers in therapeutic areas of interest and in support of Grifols existing products and innovation portfolio. Build and/or maintain relationships with key opinion leaders and gather insights to inform company strategy and innovation portfolio.

Requirements

MD with at least 8 years experience in Pulmonology and Critical Care
Advanced analytical and strategic thinking skills
Demonstrated exceptional interpersonal and communication (oral and written) skills
Excellent relationship building skills and ability to collaborate with internal and external stakeholders
Results-driven and committed to excellence in the achievement of objectives
Willingness to travel within the US and globally to attend internal and external events/conferences (15-20%)

Nice To Haves

Board Certification preferred
Prior academic position preferred
Knowledge of medical affairs within plasma/pharmaceutical industry experience preferred

Responsibilities

Serve as the therapy area expert for internal and external stakeholders. Provides expert clinical and scientific support to internal teams in the Scientific Innovation Office and commercial functions.
Support development of global and US medical affairs plans in alignment with business objectives. Contribute to commercial strategic planning globally and in the US.
Build/maintain relationships with scientific thought leaders in Pulmonology and Critical Care and related indications
Provide product and disease-specific education and training to internal stakeholders and external customers
Participate in and/or facilitate advisory boards, speaker training meetings, symposia, webinars, standalone meetings, etc
Review promotional materials and medical information letters to ensure medical accuracy
Contribute to the development and execution of publication plans and strategies
Review investigator initiated research concepts and proposals and make funding recommendations
Serve as a company ambassador during engagements with external patient advocacy organizations
Provides strategic input for business development plans and provide scientific/medical review for BD opportunities
Attends global and national medical conferences and report key findings and insights to internal stakeholders
Partner with patient advocacy, regulatory, HEOR, and market access to support US and global needs