Requirements: English
Company: TMAC
Territory includes but is not limited to: Multiple EU countries.The Regional Medical Director (RMD) is an integral member of the oncology clinical sciences group, assisting and extending Clinical Sciences across the oncology portfolio on assigned studies at the regional level.Duties and Responsibilities :Site engagement and trainingA cadence of touchpoints with sites on a regular basisMeeting with sites and presenting at PSVs, SIVsRetraining as needed (e.g., due to amendments)Addressing recruitment issuesSite identification / recruitment : Meeting with potential sites, in collaboration with CTL, to discuss the program and assess their interest.Managing patient recruitment issues by meeting with sites and troubleshooting with CTL.Answering questions from sites.Helping address site medical/clinical questions as a first line, especially for straightforward or previously addressed questions, and coordinating responses with the Medical Director for complex or new questions. This includes referencing and updating the FAQ as applicable.Medical Director should be copied on email correspondence for oversight.Assisting with eligibility assessments.Helping perform eligibility checks or address urgent eligibility questions prior to randomization.Assisting with query closure and helping sites understand requirements to close a medical query, including providing feedback for clarity improvements.Ensuring that all information needed to describe a safety event is sufficient, including:Gathering all required information in collaboration with CRA, requesting additional assessments if needed.Answering all questions and completing follow-up assessments.Managing protocol deviations by retraining sites to prevent future issues and address misunderstandings.Addressing retention issues by ensuring follow-up with patients and meeting protocol-specific requirements.Ensuring missing assessments are obtained promptly, such as LDH values in PNH studies or other key assessments in different studies, in collaboration with CRA/CTL.Collaborating with CRA to ensure laboratory reference ranges are provided for local data.Discussing potential quality issues with sites, escalating to the global medical director if unresolved.Participating in CSTs and weekly meetings or communication with the medical director.Providing clinical assistance and feedback on PI interest at the local level.Qualifications and Experience :MD required8+ years of industry clinical development experienceExpertise in Oncology, Hematology, and CardiologyStrong understanding of clinical research landscape and trial conductExcellent relationship-building skills with stakeholders and site staffAbility to work in cross-functional and diverse teamsExcellent communication and presentation skillsCritical thinking and troubleshooting skillsStrong initiative and judgment, representing Regeneron professionallyCross-cultural awareness and fluency in the primary language of the country of assignment, in addition to EnglishProficiency in Excel, Word, PowerPointWillingness to travel up to 65%, including local, regional, and international travelValid drivers license#J-18808-Ljbffr