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"Mau": Hawaiian word for always, perpetual, durable, constant"Ola": Hawaiian word for life, health, well-beingYoga as a (complementary) therapy has many benefits. Although there is not evidence that yoga can treat any disease itself, research has shown that yoga can: - help improve high blood pressure, heart rate, breathing, metabolism and body temperature. - improve strength, mobility, bone health, cardiovascular health, breathing pattern and other physiological systems and decrease pain. - enhance well-being, lower stress response, help manage pain experience and help feel more relaxed, therefore enhance quality of life. - help people living with some condition relieve their anxiety and depression. It’s also been shown to increase a sense of spiritual well-being.- help with fatigue or sleeping problems.Online yoga classes: 1/ Chair Supported Yoga for anyone recovering from injury or illness. This practice is accessible to those with limited mobility, those who may not be able to support weight standing, or those who struggle with balance and dizziness issues or with going from standing to sitting on the floor and getting up again. 2/ All levels Yoga

Develop a top-line European advocacy strategy to strengthen Incyte’s position in hematology and solid tumors with the advocacy communityProject: CML Life www.cml-life.com Foster connections with EU Patient Advocacy Groups (PAGs) that focus on hematology (CML, ALL, lymphomas, GvHD) and solid tumors (CCA, bladder, head and neck, lung...)Gather and prioritise insight regarding patient unmet needs, challenges, gaps in education/information and key patient group initiatives where there may be opportunities for collaboration. Seek opportunities to elevate the community served through compliant, forward looking, positiverelationships with these important advocacy stakeholders.Engage thoroughly in launch related activities across Europe while communicating effectively internally and externally.Develop and implement specific plans that engage patient advocacy groups in the company’s shared goal of enhancing patient access to the company‘s transformative medicines, focusing on disease and treatment education and support for capacity building of patient advocacy groups.Coordinate the delivery of information in a compliant manner through speaking engagements, written work, and ongoing communications.Effectively establish a European Patient Support Program for customers (better understanding patients’ and caregiver needs in order to address them adequately).Establish the patient experience discipline within the organization; focusing on patient supportactivities.Move conceptual support initiatives into being, with detailed and thorough execution.Proactively educate, share information, and act as an expert advisor across the cross-functionalcompany teams. Represent the patient voice in all internal efforts.Other activities include: set up EU Early Access Program, internal EU Disease Awareness weeks, audits and inspections, SOPs, Medical Information

Transition from ARIAD to Incyte with the same roles and responsibilitiesInvolved in project teams for the transfer of MAH (including transfer of safety database, E2B connectivitiy with EMA and partner, PSMF, SOP gap analysis and writing, etc)

Pharmacovigilance System Master File: maintenance and update, coordination of updates, contribution to various chapters and annexesRisk Management Plan / PBRER/: coordinating author Liaison with affiliate / vendors and oversight of PV activitiesParticipation in audits and extended support to audit and inspection preparation and response to pre-audit request / agenda, audit preparation.Pharmacovigilance Regulatory Intelligence XEVMPD, RMP Annex I EudralinkSwitzerland: Deputy Responsible Person for Pharmacovigilance, ICSR logistics and submission to Swissmedic, tracking, reconciliationAustria: Deputy Responsible Person for PharmacovigilanceTraining: Adverse event training, training administrationOthers: sharepoints set up and maintenance, reporting requirements, training matrix, SOP writing and review, data privacy

• Supervise and implement drug safety processes and collaborate with cross-functional areas globally• Set up and maintain the Pharmacovigilance System Master File in accordance with the EMA Guidelines.• Other activities include: SOP writing, Regulatory Intelligence, Regulatory requirements matrix production.• Set up of local affiliates worldwide and serve as subject matter expert: local quality system, audit preparation, CAPA preparation and resolution. Liaison between global and local Pharmacovigilance.

Coordinate planning, writing and release of safety periodic reports (PSUR, DSUR, pSUSAR) to health authorities (portfolio of about 380 products)

Coordinate complex Phase I oncology and IV dermatology projects by ensuring project delivery on time, on budget and with high quality standards.

Responsible for related marine biology activities.

Teach Mathematics, Biology, Geology, Physics and Chemistry to children between 8 and 14 years old following the French educational system and the distance-learning program (CNED)

Assist researchers and collaborate to an environmental survey “improvement and genetic biodiversity of hardwood UK native species” and a rosaceous genomics project “genetic mapping of Fragaria”.