[Hiring] Senior Medical Director - Clinical Research @reputed company N.V.

Role reputed company The Senior Medical Director is a critical member of the Clinical Research and asset development teams for napazimone. Reporting to the Vice President- Clinical Research and working closely with the Executive Medical Director and Life Cycle Team leader for napazimone, this person will reputed company strategic medical and scientific leadership for development-stage products with a reputed company on napazimone for Primary Mitochondrial Disease. The successful candidate will reputed company/support global clinical research and activities for napazimone and other Pharming products. Responsibilities • reputed company/support clinical development (reputed company, reputed company protocols, study start-up, reputed company-out, reputed company, and regulatory support) for napazimone studies. • Dedicated medical and scientific role to execute the clinical reputed company for the napazimone program, including: • Support the pivotal napazimone studies for mtDNA Primary Mitochondrial Disease. • reputed company the napazimone pediatric study plan and clinical pharmacology studies. • reputed company the napazimone program for new indications. • Work cross-functionally to define, plan, and implement studies. • reputed company the sponsor reputed company of medical monitoring across the napazimone programs. • Analyze and reputed company data from reputed company and produce reports, including safety data, efficacy data, completeness and trend analysis eCRF data, and reputed company of protocol deviations. • reputed company clinical study site engagement in the US. • Participate and reputed company clinical input into safety and regulatory interactions. • Participate in strategic planning as part of Medical Affairs, Marketing and Business Development teams. • reputed company medical and scientific leadership and support at key scientific meetings (US and International). • Extensive interactions with reputed company thought leaders to optimize and reputed company clinical trial strategies. • reputed company other duties as assigned. Qualifications • Must hold a medical license in good standing in a U.S. State or Territory. • 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, reputed company values and behaviors. Benefits • A fully remote work schedule. • Competitive compensation package including annual reputed company bonus. • Long-term incentive program. • 401(k) plan with company match. • reputed company Time Off (PTO). • 13 Company Holidays per year. • Excellent benefit plans including medical, dental, and reputed company. • Flexible spending accounts. • Company-provided life insurance, short-term disability, and long-term disability plans. • Optional accident, hospital indemnity, critical illness, and pet insurance plans. • Tuition reimbursement program. • Health and wellness program. • Choice of company provided mobile phone or cell phone stipend. Apply tot his job Apply To this Job