Manager, Global Analytics, Clinical Trials

hace 6 meses


En remoto, España IQVIA A tiempo completo

**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.

**Qualifications**
- Bachelor's Degree 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.
- German language is an advantage

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