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Consulting

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Medical Affairs or Clinical Operations related positions with a strong focus on data management
Catégorie :

Consulting

Date de dernière mise à jour :

11 octobre 2018

Lieu :

Belgium and France

CV :

Young professional with a strong sense of purpose and a natural communicator. I thrive on new experiences and challenges, learning fast, while having a tireless desire to positively and significantly impact the organization. I come with a unique mix of previous experiences in Medical and Clinical Affairs at global and regional level as a team player and team leader. I enjoy challenging the status quo and enjoy being challenged- key to accelerating transformational change. I’m all about innovation, connecting the dots, the power of data, empowering people in the healthcare industry. HBDI results: definitively yellow and red and a touch of blue and green.

Experience:

August 2017 – February 2018
Strategic Advisor – Information Management, XPE Pharma & science
Strategic and organizational assessment of the Outsourcing department.
Responsibilities:
*Assess current Services portfolio in line with client feedback and market trends (Clinical Research and eTMF solution);
*Enable business development and keep track of strategic moves in the clinical and medical area;
*Continuously scan the market to identify trends, opportunities and outperform the competition;
*Establish and review key strategic priorities and translate them in to an actionable plan;
*Facilitate, drive and monitor the execution of the strategic plan.

February 2017 – August 2017
Digital transformation consultant, XPE Pharma & Science
Coordination of Novartis Benelux Digital Transformation as part of the Commercial Excellence roadmap.
Responsibilities:
*Drive the implementation of the digital strategy across Novartis business unit for Benelux (building the basics for a long-term strategy within the Hematology Franchise);
*Co-lead pilot projects (learning process) with a focus on multichannel and digital partnership to deliver an integrated customer experience;
*Collaborate with the medical team and perform a risk assessment from a compliance and legal point;
*Establish and review key strategic priorities and translate them in to an actionable plan;
*Facilitate, drive and monitor the execution of the strategic plan.

April 2015 – June 2016
Data intelligence manager, UCB Biopharma sprl
Building the basics for a data-driven organization.
Responsibilities:
*Co-lead and define the “Big” data value chain strategy throughout the product lifecycle in order to support the company objectives, brand strategy and identify potential gaps;
*Defining Real world evidence strategy in collaboration with clinical and data Sciences teams, Compliance and Data Privacy team and Market Access and HEOR;
*Lead the integration of internal and external programs and database in order to develop a network of information;
*Assessment of the Innovative Medicines Initiative (IMI) programs with regards to their potential impact in defining the data and real world data strategy;
*Planning and follow-up of the project (for the three basic lines: Scope, Costs and Time);
*Follow-up and control of the communications between the Steering Committee and key stakeholders at local and regional level;
*Project Management Office (PMO) support, providing required data about the status of the project;
*To provide support for Quality audits (mainly internal) with regards to the “Data Integrity and compliance initiative”;
*Occasionally provide support for the review and update of the clinical study CAPA plan (as part of the Data Integrity and compliance initiative”).

July 2012 – April 2015
EU medical systems associate, UCB Biopharma sprl
Improve and optimize information and knowledge transfer through innovative approaches.
Responsibilities:
*Project leader for the implementation, maintenance, and improvement of some global medical systems and processes with high business impact in terms of information and knowledge access and sharing, collaboration and process automation;
*Provide support to or co-lead other medical affairs and/or digital related projects at European level (EU Digital Partner, MSL Excellence, LEAP, UCBCares®, CLRM, Reporting Solution, Data mining ...);
*Lead for the Medical Information Knowledge platform implementation, maintenance and continuous improvement from assessment of customer needs to provision of business solutions. (E2E Search Platform, Mobile Application Factory ...);
*Business Project manager (in collaboration with Global IT Medical) for the global roll out of key Medical systems (Internal Mobile solutions such as MedInfo iPad App, askMIKE iPad App and other technical improvement);
*Planning and follow-up of the project (for the three basic lines: Scope, Costs and Time);
*Follow-up and control of the communications between the Steering Committee and key stakeholders at local and regional level;
*Project Management Office (PMO) support, providing required data about the status of the project.
*Act as QC expert for the review of some systems related SOPs.

November 2011 – July 2012
Datavision assistant, XPE Pharma & Science
Provide support in the use of document management and data management systems.
Responsibilities:
*Support the Global Publication and Global/Local review committee in the use of Document and Database management systems such as DataVision (iEnvision), askMIKE, Infotrieve, PubMed. Update the publication database in DataVision and askMIKE;
*Coordinate and control the data collection, data cleaning, and data reporting activities for the publication team;
*Ensure proper communications with all involved parties.

Education:

September 2011
Master of bioscience engineer, free university of brussels (ulb)
Major in Bioinformatics and minor in management.
Master’s Thesis: «Bioreactor software sensors development for yeast cultures»
Extra-curricular activities:
*Trainings proposed by Stage des pôles - Biowin that intended to prepare future graduates to the bio-industrial world (e.g. Quality System in Biopharmaceutical industries, Introduction to project management);
*Voluntary work at Couleur Café festival and part-time student job.

September 2004
Bachelor of science in chemistry, free university of brussels (ulb)
Member of the student body “Cercle des Science, ASBL” management committee and A.Sc.Br.

Skills:

Entreprise domains:
*Global Publications – Process optimization, Solution implementation, Database management, Reporting solution, Datavision (iEnvision), literature intelligence, Altmetrics.
*Medical Affaires – Field force optimization, Medical content management, Multichannel strategy, Digital transformation, Solution implementation, CRM/CLRM, MSL engagement, Customers experience, KOL management.
*Medical Information – Knowledge management, IRMS, QlikView, Digital innovation, Veeva, SRL, DIA member, Data Mining, Information Intelligence.
*Project Management – Agile, Scrum.
*Clinical Affaires – 2 trainings planned via BioWin – Biophare:
o Parcours Métier Clinique: Clinical Research Associate (CRA)
o Parcours Métier Clinique : Data Management
Technical & regulatory environment:
*ICH / FDA (Mobile Apps and Medical device), GPP, GDMP, GDPR, GCP (Basic);
*Process Optimization (BPM), Enterprise Content Management, DIA Standard, Information Integrity.

Tools
*Veeva Solution, Microsoft Office, MS Project, MS Visio, DataVision, IRMS, QlikView, Mind Mapping.

Languages
French: Mother tongue
English: Professional

Personality Traits:

People oriented, Good listener, Analytical mindset, Result oriented, Strategic thinking, Team player, Multicultural personality, proactive, totally geek. Additionally, I can bring the following experiences and skills to the position:
• Strong work ethic combined with the ability to perform in high-pressure, fast-paced environments with long hours.
• Experience in traveling and living internationally and collaborating with individuals from many cultures with varied communication skills, work habits, and expectations.
• Adaptability to changing circumstances.

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