At Pfizer, we are committed to innovations that transform patients' lives, constantly striving for breakthroughs that lead to a healthier world. To fulfill our mission of delivering breakthroughs that change patients' lives, we have established clear objectives to help us meet the needs of patients. Pfizer Research & Development is the vital heart of our product pipeline, showcasing our commitment to providing life-changing medications globally. Position Overview: Oncology Field Medical Director (MD), Solid Tumors and Early Pipeline This role entails offering expert therapeutic knowledge in Solid Tumors (CRC, Melanoma, GYN) and Early Pipeline support, engaging with key medical customers and initiatives in Florida and Puerto Rico. Core Responsibilities: Strategically plan and implement medical engagement initiatives for targeted customers, collaborating with Pfizer colleagues to fulfill medical objectives. Maintain in-depth knowledge of relevant therapeutic areas and Pfizer products, providing information to both internal and external stakeholders. Act as a resource for medical information, ensuring accurate information is shared with healthcare professionals in line with Pfizer's guidelines. Contribute to the development of medical content strategies by aligning with Pfizer Medical Affairs' priorities. Ensure effective communication and collaboration amongst medical teams in headquarters and field medical colleagues. Communicate expertise through various formats, including live presentations, written materials, and virtual meetings. Enhance the patient-centricity of medical communications, keeping patient needs at the forefront. Field Medical Responsibilities: Deliver accurate, approved medical content regarding Pfizer medicines and the designated therapeutic area. Engage with priority customer segments within the assigned therapeutic space. Provide scientifically backed responses to unsolicited medical inquiries from healthcare providers, adhering to all Pfizer guidelines. Facilitate advisory boards with appropriate managerial guidance. Field inquiries from healthcare providers efficiently via established processes. Collaborate with Global Medical Affairs in identifying sites for Pfizer-sponsored clinical trials, focusing on under-represented patient populations. Support the Investigator Sponsored Research process with medical expertise. Stay updated on the latest research and congress data, cultivating expertise in the therapeutic area. Effectively communicate statistical and study design principles to relevant stakeholders. Demonstrate leadership within the territory and liaise with local Patient Advocacy Groups. Provide insights on the patient organization landscape and patient needs. Participate in cross-functional committees relevant to Medical Affairs. Represent Pfizer Medical Affairs with professionalism at clinical and professional events. Serve as a mentor for onboarding new team members and leading studies. Contribute to special projects as necessary. Qualifications: MD or DO degree required. 4+ years of relevant medical experience required. Recognized subject matter expert among peers and stakeholders. Demonstrates diverse leadership capabilities, particularly in influence and collaboration. Strong oral and written communication skills. Excellent interpersonal skills to manage multiple stakeholder demands and conflicts. Adept at managing projects in a remote setting, with a focus on prioritization and implementation. Ability to lead and adapt in a changing healthcare environment. Collaborative problem-solver capable of networking for strategic solutions. Self-starter, accountable, and results-oriented with a medical impact focus. Clinical and technical expertise is essential. Willingness to travel 60-80% of the time using a Pfizer company car. Preferred Qualifications: Familiar with SOPs and regulations relating to Pfizer and customer interactions. Previous experience in Field Medical. Work Environment: This role is field-based and involves a non-standard work schedule. EEO & Employment Eligibility: Pfizer is committed to equal opportunity employment. This position requires permanent work authorization in the United States.