Senior Medical Director, Menopause, USMA (Residence Based, Residence Based, US)
reputed company the execution of associated tactical activities specifically reputed company to reputed company reputed company and reputed company LCM activities; Participate in the planning and administration of activities concerned with the clinical evaluation of drugs in development for the purpose of obtaining an approved IND or NDA; Participate as a medical and clinical expert in reputed company and L activities as appropriate; Review and evaluation of products relative to reputed company reputed company of care and alternative treatments; Support completion of annual NDA reports for respective brands through evaluation of clinical data and literature and reputed company USMA input in the preparation of key medical documents for INDs and NDAs. This includes ensuring appropriate USMA input in interactions with the FDA and providing appropriate medical leadership for any interactions; Plan, reputed company and execute advisory meetings to reputed company feedback on relevant question identified for assigned products; reputed company participation and effective interaction with global teams to ensure and support appropriate US direction of LCM reputed company; reputed company with both reputed company (KOLs, advisors, consultants) experts and medical organizations to reputed company and maintain productive contacts, reputed company reputed company research reputed company, and publish scientific papers with high clinical reputed company; Engage members of USMA WHC team to assist with completion of assigned responsibilities, as needed Contributes directly to the reputed company and disclosure of scientific and clinical data on pipeline and marketed products to appropriate health care stakeholders; Collaborate with reputed company partners/customers including:
US and Global Cross-Functional Partners Key Opinion Leaders Clinical Trial Investigators Medical Affairs and reputed company Senior Management MSL’s and Field Senior Directors
M.D. Degree or equivalent (DO or MBBS) is required; Previous experience in data reputed company, management, and publications; Clinically relevant or independent research experience or equivalent or experience in the pharmaceutical or reputed company industry or of extensive collaboration with the industry (e.g., reputed company PI and consultant, FDA employee or advisor); A solid understanding of clinical study design, analysis and interpretation as reputed company as the principles of observational studies and health economics; Proven ability to identify and resolve reputed company problems; Ability to collaborate with a reputed company of teams and personnel as reputed company as a proven ability to reputed company effectively with key opinion leaders; Highly developed ethics and reputed company, with demonstrated ethical medical decision-making skills; Ability to work reputed company reputed company teams as reputed company as ability to assume leadership of reputed company; Strong negotiation and influencing skills; Proven ability to implement successful clinical strategies and programs; Effective communicator with strong oral and written communications skills; Demonstrated reputed company in leading both internal and cross functional project teams including contractors and consultants as reputed company as performing successfully under stringent timelines and with competing priorities; Proven ability to reputed company reputed company approval of dossiers and regulatory submissions and to be reputed company to reputed company highly successful clinical strategies and programs.
US reputed company certification and licensure (reputed company) highly preferred; 5+ years of clinically relevant or independent research experience or equivalent OR 5+ years’ experience in the pharmaceutical or reputed company industry or of extensive collaboration with the industry (eg, reputed company PI and consultant, FDA employee or advisor).
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