About Eric
Senior Project Management professional in new product development, I support Pharma, Biotech, Medtech, Start-ups, and Investment firms in optimizing the strategic and operational management of their asset portfolio to maximize patient access to innovative therapeutic solutions. I provide expertise in defining, optimizing, and executing drug/medical device/cosmetic/food supplement development strategies, along with portfolio, program, project, and alliance management services through tailored consulting engagements and interim management missions. I am mobile in Europe
French
Native or bilingual
English
Native or bilingual
Spanish
Fluent
Can work on-site
Paris (up to 50km), Lyon (up to 50km), Marseille (up to 50km), Montpellier (up to 50km), Bordeaux (up to 50km)
Experience
- EG ProjectSolutionsConsultant & Interim Manager, New Pharmaceutical Product DevelopmentPHARMACEUTICALS INDUSTRYOctober 2024 - Today (1 year and 8 months)Paris, France
- Support in defining/optimizing/executing candidate development strategy
- Support in Clinical Development strategy and execution
- Portfolio, Program, Project & Alliance Management (PMO management)
My services include: Project Management Office (PMO) set-up/optimization, Development strategy elaboration/optimization/execution for your candidates (support across the various areas of expertise required for product development from the search for candidates to commercialization), Decision-making process support, Positioning projects relative to each other based on criteria of high interest for your organization to prioritize the engagement of your human and financial resources according to the interest criteria you define, Advice on building a balanced long-term project portfolio, Search for co-development partners support (academic partners, industry partners, investors, CDMOs, CROs etc.), Operational alliance management support (establishing alliance charters, facilitating regular partnership interactions in a matrix mode, preparing decision-support materials, etc.) - NanobiotixGlobal Head of Program ManagementBIOTECHApril 2021 - October 2024 (3 years and 6 months)Paris, France
- Development and implementation of a Program Management model and of an associated PMO adapted to Nanobiotix's needs, a Biotech developing nanomedicines to treat cancers, CNS disorders and other unmet medical needs. Setting up a PMO team.
- Management of organizational changes to improve Program Management best practices
- Elaboration of early/late-stage development strategy for the Nanobiotix lead compound in multiple oncology indications. Implementation and monitoring of strategy execution with management of multiple development plans (from discovery to commercialization) across multidisciplinary matrix project teams.
- Contribution to identification and implementation of development partnerships
- NanobiotixAd interim Head of Regulatory AffairsBIOTECHJanuary 2022 - February 2023 (1 year and 1 month)Paris, France
- Line management of Regulatory Affairs Department (3 Regulatory Affairs Managers, 1 Regulatory Affairs Assistant)
- Management of interactions with Competent Authorities (EMA, FDA and PMDA) and Notified Body for the lead Nanobiotix compound (radio-enhancer) with a dual regulatory status (medicinal product/medical device) depending on the territories
- Management of organizational changes: implementation of Medical Device Regulation, reshaping of the regulatory Quality Management System
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Education
- Post-doctorateLaboratory of Molecular Genetic (CIFN)1994Post-doctorate in microbiology/molecular genetics
- PhD inUniversity Claude Bernard Lyon I/INRA of1992PhD in microbiology