Job Summary

• Contribute to the strategic planning and execution of Phase IIIb & IV trials, post-marketing requirement studies, investigator initiating or collaborative studies, serving as a study responsible physician/scientist (SRP/SRS) for select medical affairs trials.
• Partner with colleagues on real-world evidence, health economic and outcomes research, biostatistics, and work with commercial marketing colleagues through integrated evidence teams and other touchpoints to formulate and execute activities in support of the Autoantibody TA strategy across the asset, prioritizing key indications, with a focus on neuroimmunology.
• Collaborate with external investigators and thought leaders; serve as a liaison between company and clinical investigators and thought leaders, and develop credible relationships with thought leaders, medical directors, key regulatory officials, medical societies and patient advocacy organizations.

Matching Summary

Skills & Requirements

Key Requirements

• MD, DO, PhD or PharmD degree
• 8-10 years healthcare related experience
• 2 years clinical study/registry/RWE experience
• Pharma industry experience
• Clinical trial design (Phase IIIb & IV) experience

Work Rights