Chloé Bost Email & Phone Number

London, Gb

Cell and Gene Therapies/Haematology/Rare Diseases• Ensure organisation and execution of various Medical Activities:o Medical Symposium at main national haematology conference o Medical Education webinar series: development of concept and branding, topics selection addressing clinical community educational needs but also internal business needs o Advisory Board: insights leveraged to develop medical strategy • Act as Final Signatory:o Review promotional and non-promotional materials to ensure compliance to the ABPI code. o Ensure compliance for all cross-functional activities o Organise and chair quarterly compliance workshops to ensure knowledge and awareness of ABPI code within the cross-functional UK team• Lead on medical brand planning: assessment of gaps, concerns and needs, and elaboration of medical tactics for the year. Support elaboration and delivery of medical strategy• Developed a Data Dissemination strategy • Supported HTA (NICE) submission, responses to clarification questions and committee appraisal meeting: provided medical review and input into clinical responses • External stakeholders: Engagement with Thought Leaders and other HCPs • Lead of an internal Employee Resource Network that promotes diversity in the workplace: organisation of events within the company

London, United Kingdom

• MSL responsibility for London and South UK for the Cystic Fibrosis (CF) portfolio • Identify and engage with Key Opinion Leaders in CF in London & South-East UK • Provide medical and scientific support to CF centres: o Respond to requests from health care professionals (HCPs) about pipeline and licensed products o Effectively communicate complex data at all levels with clarity and simplicity o Assist centres with compassionate use requests• Develop and maintain in-depth, up-to date scientific knowledge around relevant disease areas and products• Support the UK Medical Affairs team to identify data gaps and generate real world evidence• Participated to the development, and successfully implemented 3 medical launch readiness plans based on core activities: external expert engagement, product knowledge and data dissemination, strategic insights generation• Successfully organised and delivered online educational meetings • Support medical training of Key Account Managers, new hires, and third party stakeholders

London, Royaume-Uni

• Support to the development and execution of the EU filing strategy for a new orphan drug (Cystic Fibrosis) • Supervision of the EU pivotal (phase III) clinical trials program • Elaboration and submission of complex post-marketing regulatory activities for an Orphan product in the Centralised Procedure (CP)• MHRA Good Clinical Practice (GCP) inspection: inspection readiness and function area representative

London, United Kingdom

• Regulatory management of biotechnology products within the Emerging Markets region (25 countries)• Regulatory input and expertise during cross functional strategy meetings, analyse of regulatory needs

Luton, United Kingdom

• Global regulatory management of established products (oncology & infection) within the EU • Collaboration with wide range of stakeholders to maintain pharmaceutical licences globally

London, Royaume-Uni

Paris Area, France

France

Région De Paris, France

Student job

Région De Paris, France

Managed team of a dozen employees. Supervised activities and logistics (1200 rooms for groups up to 100 people)

Doctor Of Pharmacy (Pharmd), Pharmacy

• Thesis in oncology: ‘Interest of PARP inhibitors and personalized medicine in the treatment of ovarian cancer with BRCA 1/2 mutations’ •.

Master Of Science (Msc), Drugs Regulation In The European Union

MSc in EU Regulatory Affairs

Online Self-Study Programme - Basics Of Health Economics

The Medical Plan And Tactical Implementation: Best Practices