Senior Data Verification Associate (R1088235) in Gothenburg,SE bei IQVIA™

Datum der Veröffentlichung 10/5/2019


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IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.


IQVIA has been delivering primary market research (PMR) services to the healthcare industry for over 15 years. Since 2014, IQVIA consolidated its go-to-market and delivery approach for its PMR services and formed an independent practice – Primary Intelligence. PI focuses on providing clients with a holistic solution to its research needs, by combining its primary research practices along with IQVIA’s extensive data assets PI can gives unique insights into the life sciences industry. We provide our services in 50+ countries, in 20+ languages and have a global community of 500+ expert PMR professionals as part of our PI organisation within IQVIA.

You’ll be truly part of a global community, have opportunity to work with a diverse range of cultures and hone your skills on global client projects. You’ll gain exposure to various primary research techniques and patented methodologies, state-of-the-art tool sets, pioneering data assets across numerous therapy areas and be part of one of the vibrant and fast growing IQVIA businesses. 

  • Our Delivery hub in Gothenburg, Sweden is looking for a Supervisor within the department of Data Collection, Gothenburg. We are looking for a person with a strong personal drive and good people skills. You are a problem solver who stays service minded and team oriented in a rapidly changing environment and often with challenging deadlines. You have a selling personality and you are able to analyse and organise your work independently. The main responsibility is to manage all day to day priorities, workflow and production budgets, ensuring appropriate capacity planning for DC production.

Responsibilities will include:

  • Scheduling of all Syndicated & AdHoc DC production
  • Scheduling of all panel work – monthly, quarterly and semester basis.
  • Main point of contact for our remote production outside IQVIA Medical Radar
  • Recruit and administer physicians on all panels and Syndicated/AdHoc studies
  • Continues contact and follow up with LO´s where required
  • Coordinates with production related functions within Data Sourcing, Quality Control unit, Systems unit and Client Engagement.
  • Proactively implementing changes in way of working, short and long term, as required by client commitments
  • Build long term relations with physicians and being an ambassador for IQVIA
  • Manage, motivate and develop production staff ensuring team goals are met
  • Proactively identify complex problems and needs and develop solutions/recommendations to solve problems.
  • Work with key metrics for quality, speed and efficiency to drive both internal and external client satisfaction.
  • Translation of questionnaires from English to Finnish or Danish and vice versa.
  • Prepare statistical reports and overviews necessary to make correct decisions within Data Collection.
  • Deliver high level of quality in our deliverables and follow up against produced reports
  • Quality control processing of all collected data.
  • Follow up of potential quality issues against the input source (e.g. remote Data Collection unit)
  • Coordination of QC related functions within Data Collection, Data Processing and Client Engagement.
  • Recruit and interview on CATI/CAWI studies when needed.

Desired Skills and Experience

  • Native Finnish or Danish speaker with excellent skills in the English language.
  • Near native level skills in Norwegian and/or Swedish is a great advantage.
  • You must be eligible to live and work in Sweden without visa sponsorship
  • Experience from handling a complex working environment and project coordination is an advantage.
  • Work experience in Primary Research or equal environment, experience from working with databases, quality control systems and/or a medical background will be an additional qualification of great value.
  • Proficient user of MS Excel.
  • Administrative skills and ability to multi-task and work towards deadlines is vital.
  • High school diploma is required.
  • Experience from similar positions or a Bachelor’s degree deemed to be equivalent by the employer is preferred. 

In addition to the skills and experience above, candidates interested in joining IQVIA will have:

  • A strong commitment to high quality work and an interest in rapid learning and skill development. Professional in communicating, a team player, able to collaborate within multiple projects, handle priorities with high energy levels and to maintain a proactive engaged approach to a complex process.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1088235

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