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Design Analyst

Employer
IQVIA
Location
Sofia
Salary
Competitive
Start date
19 Oct 2021
Closing date
18 Nov 2021

View more

Discipline
Information Technology, Design
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

The Design Analyst defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making. This an individual contributor role.

  • Support Design Analytics Leads in the conduct and delivery of Protocol Assessments as part of new opportunity development and on-going project delivery.  Responsibilities include working with sales, Medical and therapeutic strategy leads, and global feasibility leads and other stakeholders to understand key challenges within a protocol design, identifying and executing standard and custom analytics to pressure test protocols, and interpreting and summarizing the findings from those analytics into meaningful insights. 
  • Ensure quality and timely project deliverables
  • Partner cross functionally to present protocol assessment findings and to determine collaboratively how to apply the results
  • Ensure all relevant data is leveraged for and included in client deliverables
  • Make recommendations and suggestions to the team regarding data utilization and process implementation
  • Coordinate the collection and delivery of appropriate data and analytics from broad range of sources to address trial design related questions
  • Reconcile and interpret cross-functional data
  • Function as a subject matter expert for data sources and tools utilized within the protocol assessment process
  • Input into, review, and production of proposal text
  • Contribute to training and support of new team members
  • Participate in the continuous improvement of departmental processes and procedures
  • May participate in functional area initiatives, special project assignments and act as departmental cross functional liaison.
  • Maintain proficiency of skills and knowledge and remain current with industry trends based on current literature

 

Bachelor's degree in life sciences or related field, with 5 years’ relevant experience including demonstrable experience in acting as the main regional lead in studies or equivalent combination of education, training and experience.

 

  • Strong interpersonal skills
  • In depth knowledge of the drug development processes across all functional areas
  • Knowledge and ability to apply GCP / ICH and applicable regulatory guidelines
  • Effective presentation skills
  • Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, Excel and databases
  • Analytical skills and ability to quickly and accurately understand, access and analyze data from divergent sources to provide an assimilation of data leading to conclusions and recommendations of country ranking / site tiering / patient enrollment forecasts
  • Good written and verbal communication skills including good command of English
  • Excellent organizational and problem-solving skills
  • Effective time management skills and ability to manage competing priorities
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech
  • Extensive use of keyboard requiring repetitive motion of fingers
  • Regular sitting for extended periods of time
  • Occasional travel

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.

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