Reference #: JR5534 SUMMARY/JOB PURPOSE: Support the early-stage pipeline by working across the Medical Affairs sub-functions, including the Medical Communications, Medical Information, Medical Science Liaison, and Operations teams. This position also work with several cross functional stakeholders outside of Medical Affairs. Essential Duties And Responsibilities: Provide timely information and strategic input into Medical Affairs activities regarding early-stage pipeline, including trial awareness and implementation, publications, medical information, HEOR and field-based activities. Contribute to development of individual agent Advisory Board plans and assure successful advisory board execution with cross functional partners, opinion leaders and HCPs. Work in close collaboration with the MSL team to ensure optimal identification and support of clinical trial sites. Support field Medical Affairs in compliantly communicating pipeline product information. Work with Medical Affairs operations team to prepare for new IST programs as appropriate. Review and analyze data from relevant internal/external sources and provide insights to Medical Affairs team, Product Development Teams (PDT) and across other functions as appropriate. Serve as a scientific and medical consultant to Medical Affairs department and cross-functional colleagues. Develop deep knowledge of pipeline products, applicable treatment landscapes and competitor programs. Develop and maintain effective relationships with external experts, such as key opinion leaders, through professional associations, professional meetings, and conferences, etc., and apply their input and feedback to Medical Affairs and PDT activities. Serve in a medical capacity on the company's medical review committee (MRC) and Veeva document review platform, providing medical review, assuring accuracy of scientific and medical content and approval of materials in compliance within our corporate guidelines and governmental regulations. Serve on various other governance committees as appropriate. Develop, maintain, and ensure adherence to policies, processes and timelines in area of expertise. Participate in the planning and execution activities of Medical Affairs initiatives and activities as appropriate. Maintain clinical and specialty expertise by attending assigned PDT meetings, business team meetings, steering committee meetings, scientific congresses, etc. Seek input and alignment with internal stakeholders on program initiatives. Participate in the publications strategy, and provide scientific and clinical direction, and review and approval of materials (Datavision) for medical/scientific presentations and publications as appropriate. Provide support for other departmental and company initiatives as requested. Other duties as assigned. Supervisory Responsibilities: Co-Lead across functions within Medical Affairs to support projects No direct reports
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