Global Safety Senior Manager

Career CategorySafetyJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONIf you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching manufacturing and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of. Join us.GLOBAL SAFETY SENIOR MANAGER LiveWhat you will doLets do this. Lets change the this vital role you will work with the Therapeutic Safety Teams for safety assessment activities for medical/scientific operations. This person will also provide scientific and compliance expertise to Global Patient Safety (GPS).Search and review adverse event data literature and other safety-relevant data for the purpose of signal detection.Perform data analysis to evaluate safety signals and write up analysis results.Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the Global Safety Officer (GSO).Direct the planning preparation writing and review of safety portions of aggregate reports.Prepare presentation of the Global Safety Teams recommendations on safety issues to the cross-functional decision-making body.Assist GSO in the development of risk management strategy and activities: Provide contents for risk management plans; Develop or update strategy and content for regional risk management plans;Assist GSOs to oversee risk minimization activities including tracking of activities; Evaluate risk minimization activity; Prepare response to regulatory inquiries related to risk management plans under the guidance of GSO.Support activities related to new drug applications and other regulatory filings: Assist GSO in developing a strategy for safety-related regulatory activities; Provide safety contents for filings.Organize and direct liaison for activities with affiliates and other internal Amgen partner regarding products.Provide support for clinical trials to review and provide input to study-related documents (e.g. study protocols; statistical analysis plans; safety-related data collection forms; and design of tables figures and listings for safety data from clinical studies) and provide aggregate review of Adverse Events (AEs)/Serious Adverse Events (SAEs) from clinical trials.Undertake activities delegated by the Qualified Person for Pharmacovigilance (QPPV) as detailed in the Pharmacovigilance (PV) System Master File and maintain a state of inspection readiness.Be representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility.WinWhat we expect of youWe are all different yet we all use our unique contributions to serve patients. The professional we seek is a partner with these qualifications.RN PharmD MPH or PAExtensive direct experience in pharmacovigilance: signal detection and evaluation; data analysis interpretation and synthesis; periodic report productionKnowledge of processes and regulations for pharmacovigilance and risk managementClinical/medical research experienceThriveWhat you can expect of usAs we work to develop treatments that take care of others so we work to care for our teammates professional and personal growth and well-being.Vast opportunities to learn and move up and across our global organizationDiverse and inclusive community of belonging where teammates are empowered to bring ideas to the table and actGenerous Total Rewards Plan comprising health finance and wealth work/life balance and career benefitsLOCATION Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.Apply nowfor a career that defies imaginationIn our quest to serve patients above all else Amgen is the first to imagine and the last to doubt. Join us.Equal Opportunity StatementAmgen is an Equal Opportunity employer and will consider you without regard to your race color religion sex sexual orientation gender identity national origin protected veteran status or disability status.We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request an accommodation..Required Experience:Senior Manager Key Skills Bidding,Integration,Christmas Temporary,ABB,Elevator Maintenance,Application Engineering Employment Type : Full-Time Experience: years Vacancy: 1