Participate in strategic planning as part of Medical Affairs, Marketing and Business Development teams + Provide medical and scientific leadership and support at key scientific meetings (US and International) + Extensive interactions with academic thought leaders to optimize and develop clinical trial strategies + Perform other duties as assigned **Qualifications** + Medical license in good standing in a U.S. State or Territory preferred + 5+ years in clinical development including managing CROs + Experience in product launch, regulatory filings and FDA communications highly preferred + Strong leadership and management skills + Strong verbal and written communication skills are essential + Exceptional interpersonal skills and problem-solving capabilities + Ability to work effectively across a global matrixed organization + Travel - Include 20% travel time required for the position where travel occurs locally or internationally, if applicable + Commitment and alignment to Pharming's mission, core values and behaviors **Salary Range** Pharming takes into consideration a combination of candidate's work experience, training, and education, as well as the scope of the role, complexity, and external market and internal value when determining a salary level. **Responsibilities** + Lead/support clinical development (strategy, develop protocols, study start-up, close-out, oversight, and regulatory support) for napazimone studies + Dedicated medical and scientific role to execute of the clinical strategy for the napazimone program, including + Support the pivotal napazimone studies for mtDNA Primary Mitochondrial Disease + Lead the napazimone pediatric study plan and clinical pharmacology studies + Lead the napazimone program for new indications + Work cross-functionally to define, plan, and implement studies + Lead the sponsor oversight of medical monitoring across the napazimone programs + Analyze and oversee data from clinical trials and produce reports, including safety data, efficacy data, completeness and trend analysis eCRF data, and oversight of protocol deviations + Lead clinical study site engagement in the US + Participating and providing clinical input into safety and regulatory interactions.