Sr Clin Plan Analyst

  • Full time
  • Prague
  • Posted 3 weeks ago

Job Overview
Perform, manage and co-ordinate activities for complex opportunities/ projects. Utilize multiple data sources to perform analysis, formulate recommendations and present to internal and external stakeholders. Train and mentor junior staff and country leads. Make recommendations and lead process improvements.

Essential Functions
• Accountable to ensure IQVIA planning services are providing a competitive edge in winning new business. Take independent responsibility for the creation of complex country and/or enrollment strategies or site lists in support of opportunities including but not limited to requests for proposals, early engagements, re-bids and potentially awarded studies
• Support the development of materials related to feasibility and/or enrollment strategies or site lists for customer bid defense meetings or internal customers such as Therapeutic Strategy Leads, Medical Leads or business development
• Recommend solutions for key stakeholders and IQVIA project teams
• Prepare for planning meetings by conducting complex research into therapeutic areas using databases, scientific literature, the internet and expert medical knowledge
• Lead complex planning meetings with internal stakeholders including Medical Directors, Therapeutic Strategy Leads, Business Developers, Sales Staff and Program Directors. Present results of data gathering and analysis activities
• Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research
• Train, support and mentor new team members
• Serve as a SME for planning tools, demonstrate an depth understanding of system features and functions to know what features are best used to accomplish an accurate country, site or enrollment strategy.

• Bachelor’s Degree: Healthcare or Biological Science 
• 5 years’ related experience in clinical research. Equivalent combination of education, training and experience.
• “Clinical/project management experience is preferred.;
• General knowledge and understanding of company clinical systems, procedures and corporate standards.; 

• Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.;
• In-depth understanding of clinical research.;
• Excellent communication, organizational and interpersonal skills.;
• Fluid report writing in English.;
• Strong computer literacy, including well-developed computer skills in applicable software.;
• Ability to work independently and effectively prioritize tasks.;

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