Experience

Looking for a new project to work on.

• Computer Networking Products
• 1 - 100 Employee

• Medical Lead | Research and Development Manager

  • Jan 2023 - Present



AbbVie

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Medical Lead (Immunology- Gastro/Rheum/Derma)

  • Feb 2021 - Jul 2022

  - Set Medical Affairs strategies ensuring alignment and cross functional collaboration on key strategies, deliverables, portfolio and communication according business priorities (new launches) - Provide strategic input to the affiliate long term business plans and future local R&D plans - Ensure communication and activities are efficient and driven in compliant way - Review and Certification of Immunology medical and non-medical materials - Reinforce partnerships and engagement… Show more - Set Medical Affairs strategies ensuring alignment and cross functional collaboration on key strategies, deliverables, portfolio and communication according business priorities (new launches) - Provide strategic input to the affiliate long term business plans and future local R&D plans - Ensure communication and activities are efficient and driven in compliant way - Review and Certification of Immunology medical and non-medical materials - Reinforce partnerships and engagement with strategic external experts and Investigators - Ensure alignment with region and global strategic plans – member of regional IMM team leaders - Raise medical affairs standards - set goals, monitor performance and medical KPIs - Ensure adequate resources- recruitment, onboarding, integration, coaching and people development

• Medical Manager

  • Nov 2016 - Feb 2021

  - Lead and define strategic medical affairs activities, develop and ensure medical plans implementation aligned with brand strategy - HUMIRA, SKYRIZI and RINVOQ launch - Define medical external experts panel – mapping, profiling and segmentation - Engage in customer facing activities and develop relationships with experts and medical societies - Act as an internal scientific expert for Brand Team and In field team - Work together with market access to generate real word evidence… Show more - Lead and define strategic medical affairs activities, develop and ensure medical plans implementation aligned with brand strategy - HUMIRA, SKYRIZI and RINVOQ launch - Define medical external experts panel – mapping, profiling and segmentation - Engage in customer facing activities and develop relationships with experts and medical societies - Act as an internal scientific expert for Brand Team and In field team - Work together with market access to generate real word evidence and suuport reimbursement dossiers - Work with R&D team and Investigators in 4 clinical trials to contribute to achieve local goals and accelerate pre launch (sites identification, selection, feasibilities, and tracking performance) - Review, approval and monitor Stakeholder Interaction Plan - develop metrics report - Review and Approval VEEVA materials (promo and non promo) - Responsible for medical bubget management

• Medical Advisor

  • Oct 2014 - Nov 2016

  - Member of Task Force for HUMIRA new indication – Hidradenitis Suppurative (HS) - Work in a cross functional team, responsible for medical strategy definition and implemention of tactical plan - Define HS medical panel – external experts mapping, profiling - Define stakeholder interaction Plan - Scientific exchange and professional relationship development with key external experts, investigators and patient association - Insights collection activities – advisory boards… Show more - Member of Task Force for HUMIRA new indication – Hidradenitis Suppurative (HS) - Work in a cross functional team, responsible for medical strategy definition and implemention of tactical plan - Define HS medical panel – external experts mapping, profiling - Define stakeholder interaction Plan - Scientific exchange and professional relationship development with key external experts, investigators and patient association - Insights collection activities – advisory boards, expert panels, competitor intellenge - Brand team and In Field Team scientific training

• Medical Science Liaison

  • Jun 2012 - Oct 2014

  - Member of brand team responsible for strategy, medical launch activities and tactical plan implementation for HUMIRA launches in Ulcerative Colitis and paediatric Chron Disease. - Member of in field team responsible for account plans with sales rep and Key account managers - Implement scientific programs in field to change clinical practice - Scientific data exchange - Inform, collect and insights sharing - Define stakeholder interaction plan - Business partners scientific… Show more - Member of brand team responsible for strategy, medical launch activities and tactical plan implementation for HUMIRA launches in Ulcerative Colitis and paediatric Chron Disease. - Member of in field team responsible for account plans with sales rep and Key account managers - Implement scientific programs in field to change clinical practice - Scientific data exchange - Inform, collect and insights sharing - Define stakeholder interaction plan - Business partners scientific training



Amgen

• United States
• Biotechnology Research
• 700 & Above Employee

• Regional Medical Liaison (Oncology)

  • Nov 2008 - Jul 2012

  - Develop medical plans for pipeline, 3 launches (VEXTIBIX; NPLATE; XGEVA) and 1 mature products (Aranesp). - Development of scientific programs to change clinical practice and field implementation - Partnerships with scientific societies and scientific exchange with external experts - Oncology/Urology - Implementation/management of local clinical studies – FOCCO study - Support the implementation of international clinical trials - Member of R&D working group -site selection,… Show more - Develop medical plans for pipeline, 3 launches (VEXTIBIX; NPLATE; XGEVA) and 1 mature products (Aranesp). - Development of scientific programs to change clinical practice and field implementation - Partnerships with scientific societies and scientific exchange with external experts - Oncology/Urology - Implementation/management of local clinical studies – FOCCO study - Support the implementation of international clinical trials - Member of R&D working group -site selection, feasabilities, tracking - Internal scientific training - Member of Task Force, Cluster Teams, Business Reviews of VECTIBIX and XGEVA -National and international congress attendance (booth, competitor intelligence and insight collection)

• Clinical Research Associate

  • Sep 2006 - Nov 2008

  Regulatory submissions, study implementation, recruitment track, vendors management, investigators engagement, site monitoring and reports, participation at local/ international investigator meetings were the main activties related to 3 clinical trials (phase II/III) in Oncology and Nephrology.



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Clinical Research Associate

  • Mar 2004 - Sep 2006

  Site feasibilities, investigator/sites selection, protocol implementation, monitoring activities, investigator meetings, recruitment tracking and investigators engagement were the main activities related to 4 clinical trials (phase II/III) - Psychiatry, Neurology and Cardiology. Site feasibilities, investigator/sites selection, protocol implementation, monitoring activities, investigator meetings, recruitment tracking and investigators engagement were the main activities related to 4 clinical trials (phase II/III) - Psychiatry, Neurology and Cardiology.



Abbott

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Clinical Research Associate - Rheumatology

  • Nov 2002 - Jan 2004

  Reporting to Medical Director, Regulatory submissions, protocol implementation, clinical site monitoring activities, international and national investigator meetings, recruitment tracking and clinical research investigators engagement were the main activities developed in this position. Member of HUMIRA task force, sharing insights and working with commercial/marketing team to contribute to HUMIRA successful launch. Reporting to Medical Director, Regulatory submissions, protocol implementation, clinical site monitoring activities, international and national investigator meetings, recruitment tracking and clinical research investigators engagement were the main activities developed in this position. Member of HUMIRA task force, sharing insights and working with commercial/marketing team to contribute to HUMIRA successful launch.