Senior Director, Global Medical Affairs, Solid Tumors Position Available In New York, New York
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Job Description
Job ID :
506dc5bc-a09f-4a70-ae5b-f51a5e4e6637ResponsibilitiesThis pivotal (Senior/Executive) Director – Solid Tumours Global Medical Affairs role will focus specifically on Solid Tumors and play a critical part in shaping our pipeline strategy and maximizing the lifecycle of our assets. You will be instrumental in driving our investigator-sponsored / collaborations studies strategy, ensuring the generation of robust data to support both early and late-stage clinical development. You will bring a proactive approach, actively seeking out opportunities and engaging with investigators and sites to foster strong partnerships and gain valuable insights. Reporting to the Vice President and Head of Global Medical Affairs – Solid Tumors, you will operate at a global level, collaborating cross-functionally with Clinical Development, Clinical Operations, Biostatistics, clinical Pharmacology, Preclinical and Translational Medicine, Regulatory Affairs, Safety, Pharmacovigilance, Access and Commercial teams. Your deep understanding of the solid tumors landscape, coupled with your strategic thinking and proactive engagement style, will be crucial in driving our success. Responsibilities include, but are not limited to:
Lead clinical data generation strategy and execution for collaboration and independent research programs/trials.
Gather clinical/medical/scientific insights to optimize trial implementation.
Identify and engage qualified investigators with strong recruitment potential.
Ensure adherence to safety standards and maintain high-quality clinical data.
Collaborate with cross-functional teams to support successful trial execution.
Provide clinical/medical expertise to support trial feasibility, ethics approvals, and site selection.
Ensure compliance with regulatory standards, GCP, and internal policies.
Act as a scientific/clinical/medical expert in interactions with medical experts.
Support safety monitoring, pharmacovigilance, and risk mitigation in trials.
QualificationsEssential Requirements:
MD., Ph.D. requiredAt least 5 years of clinical development experience in the pharmaceutical industry in medical affairs / clinical developmentDemonstrate an understanding of regulatory requirements and policies, procedures, and guidelines pertaining to clinical trials.
Ability to manage clinical trials from a medical/scientific perspectiveExcellent communication and stakeholder engagement skillsAgility to work across different therapeutic areasProficiency in English and local languageAbility to travelExperience in Breast Cancer (Oncology) Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Menarini Stemline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran
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