Responsibilities: • Under general direction, serves as medical expert and contributes to strategic product plan for the region/country • Implements strategy for scientific interactions with the medical community including key opinion leaders and patient advocacy groups • Supports medical affairs operations on logistical planning and implementation of projects, including supporting and delegating activities to ensure prompt turnaround and project success • Coordinates the review of Investigator Initiated Research (IIR) study proposals • Serves as medical consultant and supports commercial, marketing and sales organizations Qualifications: • Degree in nursing, pharmacy or advanced degree in science/medicine (MD, PhD, PharmD) preferred • 5+ years' relevant pharmaceutical/ biopharmaceutical industry experience • General clinical trial experience • Knowledge of therapeutic specialty area Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.