Freelancer profile translated to English.
Back to original languageAbout Emma
Doctor of Pharmacy, defended thesis in November 2021, graduated with a Master 2 in Quality Assurance and a specialized Master's as a Medical Science Liaison. I have 7 years of experience in the pharmaceutical industry.
Within this field, I have had the opportunity to hold various positions in diverse departments. My experience spans Regulatory Affairs, Quality Assurance, Supply Chain, Pharmacovigilance, Marketing, and most recently, Medical Affairs.
Over the past four years, I had the privilege of working within the Medical Affairs department of ViiV Healthcare (a Pfizer & GSK joint venture) as a Medical Science Liaison. This role allowed me to develop a wide range of skills, including scientific data analysis, creation and writing of scientific and marketing content, simplification and dissemination of medical data to healthcare professionals and/or the general public, and external and internal written communication related to medical and scientific content.
I also hold a DIU (University Diploma) related to the management of HIV infection. Therefore, I am particularly qualified in infectiology, complementing my skills as a Doctor of Pharmacy, as well as my medical, pharmaceutical, and pharmacological expertise.
Today, I am particularly enthusiastic about launching my freelance activity, which will provide me with the opportunity to apply all the skills acquired over the past seven years, without being tied to a specific domain or task.
French
Native or bilingual
English
Native or bilingual
Spanish
Conversational
Remote only
Primarily works remotely
Experience
- ViiV HealthcareDoctor of Pharmacy / Medical Science LiaisonPHARMACEUTICALS INDUSTRYNovember 2021 - March 2025 (3 years and 4 months)Paris, FranceReactive interaction and communication of scientific and medical information to healthcare professionals: providing balanced, non-promotional scientific and medical information based on expert needs, through individual interviews or meetings.Development and writing of content for scientific partnerships aimed at developing clinical research.Interface between the medical and scientific community and the medical department.Interaction and communication with healthcare professionals regarding drug safety issues and elements related to medical study projects.Providing the company with an in-depth understanding of clinical practices and the needs of healthcare professionals and patients, useful for implementing relevant drug development plans.Support for medical representatives in response to their scientific questions and contribution to their knowledge development through the creation of marketing content.Scientific responsibility for all medical and marketing events: development of the scientific program, preparatory discussions in compliance with strategy, ethics, and marketing campaign.Public speaking following the implementation and development of scientific and marketing content during scientific meetings and symposia at national and international congresses.Establishment and management of scientific expert groups.Scientific watch of products, pathologies, and competitors: bibliographic watch, national/international congresses, and associated data analysis.
- ViiV Healthcare,Medical Science Liaison - HIVPHARMACEUTICALS INDUSTRYNovember 2021 - March 2025 (3 years and 4 months)Paris, France• Disseminated balanced, non-promotional scientific and medical data to healthcare professionals via expert meetings and individual interviews,• Developed scientific partnerships with HCPs/KOLs to support clinical research,• Produced medical writing content, performed scientific popularization, translated medical documents,• Authored and translated HIV clinical trial content, ensuring scientific accuracy and accessibility,• Interface between the medical/scientific community and internal Medical Department,• Simplified complex scientific data for diverse audiences and oversaw medical data dissemination,• Provided strategic insights on clinical practices and patient needs to support drug development plans,• Supported field teams with scientific expertise and contributed to their ongoing medical training,• Led the scientific strategy, ethics alignment, and content development for medical and marketing events,• Created and edited medical and marketing materials aligned with portfolio goals,• Delivered public presentations on scientific and medical topics at national and international conferences,• Established and coordinated scientific expert groups, advisory boards, speaker programs, to support ongoing medical engagement,• Analyzed competitor data and congress findings on pathologies to guide internal strategy.
- Strategiqual SAS,Quality and Compliance ConsultantPHARMACEUTICALS INDUSTRYNovember 2020 - November 2021 (1 year)Paris, France• Reviewed and validated medical training, promotional/non-promotional materials for MSLs and sales teams (Lilly),• Delivered training sessions on clinical trial data and developed medical training plans,• Designed and implemented documentation systems and marketing materials to support promotional activities (Daiichi Sankyo),• Conducted external audits of medical information, pharmacovigilance systems, promotional activities, and drug distribution operations,• Oversaw compliance and promotional activities related to medical product distribution, including management of complaints, deviations, temperature excursions, and reprocessing,• Edited and finalized annual Product Quality Reviews (PQRs) for Pfizer, Ipsen, BMS, and Biogen,• Drafted and submitted Shortage Management Plans for BMS, Kyowa Kirin, and Sandoz,• Prepared and tracked corrective actions and CAPAs following regulatory inspections.
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Education
- Doctor of PharmacyUniversité Paris Descartes2021Thèse de Docteur en Pharmacie
- Specialized Master 2 in Pharmaceutical Risk and Quality ManagementUniversité de Bordeaux - Faculté de Pharmacie2020