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Référence :


Lieu :

Région parisienne

Descriptif :

The QuintilesIMS NEMEA Real-World Evidence Solutions (RWES) team is a fast-growing and successful services business of around 150 people mainly located across Northern Europe that delivers real world evidence projects to our pharmaceutical and healthcare clients.

We have direct access to the world’s most comprehensive medical data and information and a large team of Epidemiologists, Programmers, Project Managers, Doctors, Pharmacists and Statisticians. In addition, we work alongside health economic, consulting and research teams to deliver deep insights into product safety, efficacy, cost, value for money and affordability. We are one of only a few organizations that integrate real-world evidence solutions (RWES), health economics, outcomes research, market access and management consulting both at national and international level.

Globally, the RWI team operates in over 20 countries and comprises more than 1,000 staff members.

Overview of the role

QuintilesIMS has developed a strong network of partners both in the academic field and the consultancy industry. QuintilesIMS is currently expanding and is thus seeking a talented individual for a consultant role

The primary responsibilities are:

• Contribute to the design, execution and reporting of pharmacoepidemiological studies, especially Post Authorisation Safety Studies (PASS) under standard and novel epidemiological study designs
• Lead or contribute to the writing of study protocols and study reports
• Interpret and write-up results of epidemiological analyses
• Manage projects to ensure they are delivered successfully and in a timely manner, including supporting client management
• Conduct and write literature reviews in support of study proposals and protocols
• Prepare abstracts, manuscripts and/or presentations to conferences for internal and external projects
• Support development of draft proposals based on client RFPs and supporting information
• Review and analyse client requirements, research question or problems in order to deliver optimal solutions to meet their needs
• Support senior staff on specific business initiatives, as required


Essential qualifications
• MSc in Epidemiology, Pharmacoepidemiology, or Biostatistics; MPH, MD or PharmD with experience in consultancy, epidemiology or drug safety
Essential experience

• 2+ years experience working with a research team in a consulting, pharmaceutical, or CRO setting
• Must possess strong project management and organizational skills, exceptional analytical and communication skills (written and oral)
• Ability to prioritize and manage multiple tasks simultaneously to meet deadlines
• Proven record delivering projects on schedule and within budget
• Excellent presentation and client facing skills
• Preferred: experience analyzing secondary data sources including insurance claims, EMR and pharmacy databases.

Essential personal skills and behaviours

• Fluency in English (spoken and written); strong business/scientific written English is vital
• Strong written and verbal communication skills and the ability to build strong consultative business relationships
• Excellent presentation and client influencing skills
• Good team based interpersonal skills but also able to work independently
• A commitment to working collaboratively and effectively with others in and across the team to accomplish goal

ADRESSEZ-NOUS VOTRE CANDIDATURE avec votre CV et votre lettre de motivation à :

Contact :

17 bis place des Reflets

92099 La Défense cedex

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