Study-level Clinical Development Leadership - Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study team(s) that is scientifically rigorous and aligns with company objectives. - Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring. - Lead peer-to-peer interactions with investigators. - Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities. - Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team. Strategic Guidance, Clinical Insights & Interpretation - Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders. - Maintains a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans. Basic Qualifications. Medical degree Required with 4 years experience. Clinical Development experience required 2-4 years industry experience required. Preferred Qualifications. Late-stage clinical development experience preferred. Hematology experience preferred. Board certified/eligible in oncology or equivalent preferred. Organizational Relationships. Reports to Global Development Lead or Senior/ Executive Medical Director. Partners closely subject matter experts within cross-functional study team, Pfizer Oncology Division and counterparts in other divisions within Pfizer.