Provider of information solutions enhancing the performance of science, health, and technology professionals, 9k employees
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Senior Product Development Manager
As part of product management team in PharmaBioTech division, Medical Products subdivision supported roadmap and maintenance development for flagship product as well as SDLC governance for a new product. Acted as Voice of Quality (GxP) in Product Management and Development Team. Bridged technology and business stakeholders.
- Served as Product Owner for SCRUM development team for two products (Quosa and Quosa PV).
- Served as Product Manager for Quosa for eight months, raising NPS from previous 12 months average of 1 up to 7, and then 9.
- Wrote product specifications for refactoring effort of the QUOSA product, including security and regulatory requirements considering GxP needs of target market.
Life Sciences Consultant
Member of multidisciplinary professional services team; owned bibliographic products non-standard RFP/RFI’s and sales engineering across EMEA; advised on product capabilities to integrate into complex projects, expanded skill and responsibility as PV, Data Quality, Data Security and GxP software compliance SME for team and PBT Division.
- Performed GxP assessment and wrote the functional/non-functional specification to fulfil regulatory requirements for a new product (Quosa PV).
- Contributed to new Pharmacovigilance’s Go To Market strategic plan for the PBT division.
- Devised methodology for formulating and validating queries for PV purposes on Abstract & Index databases (2 conference presentations and a whitepaper, knowhow incorporated on EMBASE PV Wizard).
- Implemented (including validation) migration of large Literature Current Awareness for Medical Affairs/Medical Information maintaining complex Copyright compliance (Sanofi/Pasteur/Zentiva).
- Succeeded in driving the implementation of a Quality Management System and the creation of a Quality Manager position.
- Multiple publications, industry articles eg:
- Pharma R&D Today , The EMA’s literature screening service and pharma and Dos Anjos, J. 2015,
- “Complexities and new potential in Pharmacovigilance”, Pharmaceutical Market Europe, November 2015, pp. 44-45
- Multiple presentations and webinars:
- Electronic Document Management Conference 2016 (DIA)
- Pharmaceutical Information and Pharmacovigilance Association Conference 2016 (PIPA)
- Risk Management and Pharmacovigilance Summit 2017
Solutions Specialist
Elicitation of relevant requirements and cross-referenced with product functionalities. Developed pilot installations to validate value proposition. Collaborated with cross-functional teams on the new features required by customers. Supported account team in demonstrating product value and ROI in support of significant customer contract negotiations (sale, up-sale or renewal).
- Deployed and supported large Drug Safety literature screening project (Sanofi global PV).
- Planned, executed, and delivered multiple data migration projects, including programming for data conversion and migration validation.
- Performed query conversion and harmonization for 800 medicinal products, including programming of string generation ready for import (Sanofi).
- Became PV domain SME for both Product and PharmaBioTech division.