%3Cfont size=%223%22%3E%3Cdiv style=%22%22%3E%3Cfont face=%22Verdana%22%3E%3Cb style=%22%22%3ERole Purpose%5C:%3C/b%3E%26nbsp;%3C/font%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EResponsible for managing the planning, implementation, execution, coordination and overall direction of clinical research projects on program level in Europe related to specific products or topics according to internal and external regional requirements.%26nbsp; Supervises/manages Clinical Research Specialists (Project Managers and Lead CRA's) assigned to specific clinical research projects within the clinical program, may also be responsible for specific study sites.%26nbsp; Interacts with various internal/external groups/departments in Europe and USA to facilitate progress and completion of clinical research projects.%26nbsp; Assists Director in budget administration.%26nbsp; Frequently interacts with subordinate specialists, European investigators/customers and other peer group managers. Assists in training of new personnel.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cb%3E%3Cfont face=%22Verdana%22%3E%3Cbr%3E%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cfont face=%22Verdana%22%3E%3Cb%3EJob Functions%5C:%26nbsp;%3C/b%3E%26nbsp;%3C/font%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDeliver Clinical Trial studies while ensuring compliance with regulations and company SOPs%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EManage/supervise pre-study visits, contract negotiation within established guidelines, establishing and maintaining contact with key hospital departments as required (e.g. Purchasing, Laboratories, Diagnostics, supporting disciplines, control the device accountability during trials);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAdminister and supervise trial implementation including preparation/submission of Ethics Committee/Institutional Review Board materials and MoH submissions%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDrive process improvement and initiate corrective actions to resolve any compliance issues%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDevelop team members and assure all have training plans and development planes.%26nbsp;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EProvide leadership and guidance on issues where cross functional/BU consistency is essential for good clinical practice.%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ELeads and/or participates in various global TMTT projects related to clinical trials and clinical organization.%26nbsp;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise preparation and execution of site personnel training including Edwards SOP´s, preparation/maintenance of study documents, completion of forms, understanding of examinations/assessments required%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise/Manage site enrollment progress, study compliance and development of resolution action plan together with assigned Clinical Research Specialists (PM / Lead CRA)%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise/Manage preparation, documentation, monitoring and distribution of contract obligations including financial obligations and ensuring that trial contract obligations are met in a timely manner. The process must be followed until the contract signature is obtained from both parties%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EServing as key contact to assigned Clinical Research Specialists (PM and Lead CRA) throughout the study process until study termination and study closeout;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EMaintaining regular contact with country sales organization for the exchange of study related information%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EManages/Partners with assigned CRO personnel, Associate/ Clinical Research Specialists or any additional personnel specifically hires for the study monitoring;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAssist in preparation of clinical data presentations for regulatory submissions, conferences and study meetings (Data locks, Executive Committees, DSMB, CEC, Steering Committees);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EParticipate and support screening process in close collaboration with R%26amp;D, screening team and CS.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22font-family%5C: Arial;%22%3E#LI-MC1%3C/div%3E%3C/font%3E!|!!!%3Cfont size=%223%22%3E%3Cdiv style=%22%22%3E%3Cfont face=%22Verdana%22%3E%3Cb style=%22%22%3ERole Purpose%5C:%3C/b%3E%26nbsp;%3C/font%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EResponsible for managing the planning, implementation, execution, coordination and overall direction of clinical research projects on program level in Europe related to specific products or topics according to internal and external regional requirements.%26nbsp; Supervises/manages Clinical Research Specialists (Project Managers and Lead CRA's) assigned to specific clinical research projects within the clinical program, may also be responsible for specific study sites.%26nbsp; Interacts with various internal/external groups/departments in Europe and USA to facilitate progress and completion of clinical research projects.%26nbsp; Assists Director in budget administration.%26nbsp; Frequently interacts with subordinate specialists, European investigators/customers and other peer group managers. Assists in training of new personnel.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cb%3E%3Cfont face=%22Verdana%22%3E%3Cbr%3E%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cfont face=%22Verdana%22%3E%3Cb%3EJob Functions%5C:%26nbsp;%3C/b%3E%26nbsp;%3C/font%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDeliver Clinical Trial studies while ensuring compliance with regulations and company SOPs%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EManage/supervise pre-study visits, contract negotiation within established guidelines, establishing and maintaining contact with key hospital departments as required (e.g. Purchasing, Laboratories, Diagnostics, supporting disciplines, control the device accountability during trials);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAdminister and supervise trial implementation including preparation/submission of Ethics Committee/Institutional Review Board materials and MoH submissions%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDrive process improvement and initiate corrective actions to resolve any compliance issues%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EDevelop team members and assure all have training plans and development planes.%26nbsp;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EProvide leadership and guidance on issues where cross functional/BU consistency is essential for good clinical practice.%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ELeads and/or participates in various global TMTT projects related to clinical trials and clinical organization.%26nbsp;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise preparation and execution of site personnel training including Edwards SOP´s, preparation/maintenance of study documents, completion of forms, understanding of examinations/assessments required%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise/Manage site enrollment progress, study compliance and development of resolution action plan together with assigned Clinical Research Specialists (PM / Lead CRA)%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervise/Manage preparation, documentation, monitoring and distribution of contract obligations including financial obligations and ensuring that trial contract obligations are met in a timely manner. The process must be followed until the contract signature is obtained from both parties%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EServing as key contact to assigned Clinical Research Specialists (PM and Lead CRA) throughout the study process until study termination and study closeout;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EMaintaining regular contact with country sales organization for the exchange of study related information%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EManages/Partners with assigned CRO personnel, Associate/ Clinical Research Specialists or any additional personnel specifically hires for the study monitoring;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAssist in preparation of clinical data presentations for regulatory submissions, conferences and study meetings (Data locks, Executive Committees, DSMB, CEC, Steering Committees);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EParticipate and support screening process in close collaboration with R%26amp;D, screening team and CS.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22font-family%5C: Arial;%22%3E#LI-MC1%3C/div%3E%3C/font%3E!|!!!%3Cfont size=%223%22%3E%3Cdiv style=%22%22%3E%3Cb style=%22%22%3E%3Cfont face=%22Verdana%22%3ERequired Education/Skills/Experience%5C:%26nbsp;%26nbsp;%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EEnglish (written %26amp; spoken), at least one additional European language desired%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EComputer skills - Microsoft Office (Word, Excel, Access, Powerpoint), Internet%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EFamiliarity with hospital environment%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EGood communication and organizational skills%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EThorough, conscientious and results oriented working style%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ETeam oriented%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EIndependent judgment skills %26amp; action orientation for obtaining required results%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cb%3E%3Cfont face=%22Verdana%22%3EExperience%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3E7+ years managing clinical studies or related clinical programs in European Union specifically on medical devices (preferred);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAdvanced knowledge of European and international regulations of Good Clinical Practice (GCP), experience with Class II %26amp; III medical devices preferred, documented current continuing education in clinical research monitoring or experience in Clinical Research;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EProject management experience;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervision or mentoring of subordinates;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EGood orientation to the team working.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22font-family%5C: Arial;%22%3E%3Cbr%3E%3C/div%3E%3C/font%3E!|!!!%3Cfont size=%223%22%3E%3Cdiv style=%22%22%3E%3Cb style=%22%22%3E%3Cfont face=%22Verdana%22%3ERequired Education/Skills/Experience%5C:%26nbsp;%26nbsp;%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EEnglish (written %26amp; spoken), at least one additional European language desired%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EComputer skills - Microsoft Office (Word, Excel, Access, Powerpoint), Internet%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EFamiliarity with hospital environment%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EGood communication and organizational skills%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EThorough, conscientious and results oriented working style%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ETeam oriented%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EIndependent judgment skills %26amp; action orientation for obtaining required results%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cb%3E%3Cfont face=%22Verdana%22%3EExperience%3C/font%3E%3C/b%3E%3C/div%3E%3Cdiv style=%22%22%3E%3Cul%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3E7+ years managing clinical studies or related clinical programs in European Union specifically on medical devices (preferred);%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EAdvanced knowledge of European and international regulations of Good Clinical Practice (GCP), experience with Class II %26amp; III medical devices preferred, documented current continuing education in clinical research monitoring or experience in Clinical Research;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EProject management experience;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3ESupervision or mentoring of subordinates;%3C/div%3E%3C/font%3E%3C/li%3E%3Cli%3E%3Cfont size=%223%22 face=%22Verdana%22%3E%3Cdiv%3EGood orientation to the team working.%3C/div%3E%3C/font%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv style=%22font-family%5C: Arial;%22%3E%3Cbr%3E%3C/div%3E%3C/font%3E!|!!!%3Cfont size=%223%22 face=%22Arial%22%3E%3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22 lang=%22en-US%22%3E%3Cspan style=%22font-weight%5C:bold;background%5C:white%22%3EAbout Edwards%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3EEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world%27s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 10,000 individuals worldwide.%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:Arial;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3E%26nbsp;%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3EFor us, helping patients is not a slogan - it%27s our life%27s work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life. Edwards is an Equal Opportunity/Affirmative Action employer including Minorities, Females, Protected Veterans, and Individuals with Disabilities.%3C/span%3E%3C/p%3E%3C/font%3E!|!!!%3Cfont size=%223%22 face=%22Arial%22%3E%3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22 lang=%22en-US%22%3E%3Cspan style=%22font-weight%5C:bold;background%5C:white%22%3EAbout Edwards%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3EEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world%27s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 10,000 individuals worldwide.%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:Arial;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3E%26nbsp;%3C/span%3E%3C/p%3E %3Cp style=%22margin%5C:0in;font-family%5C:verdana;font-size%5C:12.0pt;color%5C:black%22%3E%3Cspan style=%22background%5C:white%22%3EFor us, helping patients is not a slogan - it%27s our life%27s work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life. Edwards is an Equal Opportunity/Affirmative Action employer including Minorities, Females, Protected Veterans, and Individuals with Disabilities.%3C/span%3E%3C/p%3E%3C/font%3E!|!Clinical Affairs!|!Clinical Affairs!|!Europe, Middle East, Africa, Canada (EMEAC)-Switzerland!|!Europe, Middle East, Africa, Canada (EMEAC)-Switzerland!|!!|!!|!false!|!308442!|!308442!|!true!|!308442!|!false!|!Submission for the position%5C: Sr, Manager Clinical Affairs, TMTT - (Job Number%5C: 019960)!|!false!|!308442!|!false!|!true!|!https%5C://edwards.taleo.net/careersection/jobdetail.ftl?job=019960%26lang=en!|!Sr, Manager Clinical Affairs, TMTT!|!true!%24!ftlerrors!|!!|!descRequisition.size!|!1!|!descRequisition.nbElements!|!1!|!descRequisition.isEmpty!|!false!|!descRequisition.hasElements!|!true!|!pSessionTimeout!|!0!|!pSessionWarning!|!0!|!pBeaconBeat!|!0!|!focusOnField!|!!|!csrftoken!|!nfWUWEmn6qO//ATOcnNnqaBUxWBNkF1ne178ubMapBM=!|!emptyListToken!|!!|!isListEmpty!|!false!|!listCount!|!!|!displayCalloutInLegend!|!false!|!addThisRequired!|!true!|!jobboardListPageTitle!|!!|!commonDescriptionForAddThis!|!!|!alreadyAppliedColumnDisplayed!|!false!|!displayDraft!|!!|!displaymessage!|!false!|!initialHistoryPage!|!1!|!restoreInitialHistoryOnRefresh!|!false!|!applicationCandidateNo!|!!|!calloutPageDisplayed!|!false!|!descriptionLogginMandatory!|!false!|!displayAsMainHeader!|!false!|!displayListingsPerPage!|!false!|!displayUrgentNeed!|!!|!isApplicantUser!|!true!|!jobsPerPageCaption!|!Job {0} out of {1}!|!listEmptyIsApplicantUser!|!true!|!listLabels!|!!|!listLocales!|!!|!requisitionno!|!308442!|!interfaceIdForTimeZone!|!requisitionDescriptionInterface!|!isJobCartActionDisplayed!|!true!|!openDescFrom!|!default!|!serializedCriteria!|!!|!sortby!|!11!%24!requisitionDescriptionInterface!|!!|!!|!!|!!|!!|!Apply for this position online!|!Apply by Email!|!Apply to this position by email!|!Add this position to the job cart!|!!|!Job Description!|!About Edwards!|!Tell us about a friend who might be interested in this job. All privacy rights will be protected.!|!false!|!Tell us about a person who might be interested in working for our organization. All privacy rights will be protected.!|!true!|!!!1. Create your myReferral account www.edwardsmyreferral.com%0A %3Cbr%3E%0A 2. Click sign-up%0A %3Cbr%3E%0A 3. Enter your Edwards email address and employee ID%0A %3Cbr%3E%0A 4. Start referring%0A%3Cbr%3E%0A Questions? Contact us at: Edwards_my_referral@edwards.com!|!Apply for this position online!|!Apply to this position by email!|!Add this position to the job cart!|!!|!!|!!|!