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Evidence Generation Strategy Lead - Epilepsy, Slough
Client:
UCB Location:
Slough, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
00be1ed4b777 Job Views:
85 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Make your mark for patients We are looking for an
Evidence Generation Strategy Lead
who is agile and innovative to join us in our
Patient Value Neurology Group , based at our HQ in
Brussels ,
Belgium
or
Slough, UK . About the role Accountability for strategic planning and leading regional Europe Epilepsy and Rare Syndrome RWE studies/ Evidence Generation (EG). Activities across the products/indications as defined within the Neurology therapeutic area in alignment with global/ regional and local EG strategy, Launch and Market Access needs. What you’ll do Providing expert input to the evidence generation initiatives planned and managed by local cross-functional teams across EU, supporting Launch and Market Access activities Helping to shape the use and acceptance of RWE in the external environment, collaborating with relevant internal roles Providing subject matter expert input in Clinical Study Teams and RWE practice Membership in relevant regional and global teams, including leading on the EU Integrated Strategic Evidence Generation group Acting as a primary contact person and owner for RWE EU ERSO studies for vendors and internal stakeholders, including budget allocation Designing study concepts, translating them into study protocols, co-working with all internal cross-functional roles Guiding Clinical Development decisions concerning the selection of appropriate clinical/patient-reported endpoints, target patient populations and RWE tool Overviewing and accountability for the execution of the RWE studies and other EG projects, including interim and final results delivery, interpretation and communication of outcomes for internal decision making Developing and executing proper and in-time dissemination of the evidence gained in peer-review journals and congresses, based on the Strategical Publication Plan and according to Patient Value Brand Plans Collaborating with local medical teams and RWE partners identifying potential countries and sites for participation in RWE studies, including alignment with Key Opinion Leaders and professional organizations, organization of Scientific Advisory Boards Who you’ll work with Working in close collaboration with all cross-functional roles; RWE Practice, Clinical Development, Patient Safety, Market Access, Data Analytics, Medical Affairs. Collaborating with Global Medical Product Leads in RWE studies and Evidence Generation Interested? For this position you’ll need the following education, experience and skills Educated to a minimum of MSc Significant experience in pharmaceutical industry. Experience in medical affairs/RWE and preferably some experience in R&D/clinical development and publications Comprehensive knowledge of legal & regulatory requirements in R&D, including post-marketing research, NIS, other RWE Excellent understanding of clinical practice and RWE generation methodology Ability to translate pharma trends and health care ecosystem trends into opportunities through RWE generation Leading & Influencing matrix organization for patient value & Impact Proven leadership ability of internal and external cross-functional teams Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
#J-18808-Ljbffr
Client:
UCB Location:
Slough, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
00be1ed4b777 Job Views:
85 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Make your mark for patients We are looking for an
Evidence Generation Strategy Lead
who is agile and innovative to join us in our
Patient Value Neurology Group , based at our HQ in
Brussels ,
Belgium
or
Slough, UK . About the role Accountability for strategic planning and leading regional Europe Epilepsy and Rare Syndrome RWE studies/ Evidence Generation (EG). Activities across the products/indications as defined within the Neurology therapeutic area in alignment with global/ regional and local EG strategy, Launch and Market Access needs. What you’ll do Providing expert input to the evidence generation initiatives planned and managed by local cross-functional teams across EU, supporting Launch and Market Access activities Helping to shape the use and acceptance of RWE in the external environment, collaborating with relevant internal roles Providing subject matter expert input in Clinical Study Teams and RWE practice Membership in relevant regional and global teams, including leading on the EU Integrated Strategic Evidence Generation group Acting as a primary contact person and owner for RWE EU ERSO studies for vendors and internal stakeholders, including budget allocation Designing study concepts, translating them into study protocols, co-working with all internal cross-functional roles Guiding Clinical Development decisions concerning the selection of appropriate clinical/patient-reported endpoints, target patient populations and RWE tool Overviewing and accountability for the execution of the RWE studies and other EG projects, including interim and final results delivery, interpretation and communication of outcomes for internal decision making Developing and executing proper and in-time dissemination of the evidence gained in peer-review journals and congresses, based on the Strategical Publication Plan and according to Patient Value Brand Plans Collaborating with local medical teams and RWE partners identifying potential countries and sites for participation in RWE studies, including alignment with Key Opinion Leaders and professional organizations, organization of Scientific Advisory Boards Who you’ll work with Working in close collaboration with all cross-functional roles; RWE Practice, Clinical Development, Patient Safety, Market Access, Data Analytics, Medical Affairs. Collaborating with Global Medical Product Leads in RWE studies and Evidence Generation Interested? For this position you’ll need the following education, experience and skills Educated to a minimum of MSc Significant experience in pharmaceutical industry. Experience in medical affairs/RWE and preferably some experience in R&D/clinical development and publications Comprehensive knowledge of legal & regulatory requirements in R&D, including post-marketing research, NIS, other RWE Excellent understanding of clinical practice and RWE generation methodology Ability to translate pharma trends and health care ecosystem trends into opportunities through RWE generation Leading & Influencing matrix organization for patient value & Impact Proven leadership ability of internal and external cross-functional teams Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
#J-18808-Ljbffr
