Global Analyst – Clinical Trial Analytics in Brazil
IQVIA
- São Paulo - SP
- Permanente
- Período integral
Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities and projects. Perform data mining and analysis, formulate recommendations and present to internal and potentially external stakeholders.Essential Functions
- Accountable to ensure IQVIA planning services are providing a competitive edge in winning new business. Under supervision and close mentoring, make recommendations for IQVIA commitments of future studies by delivering accurate and robust country, site or enrollment strategies 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 or site lists or enrollment strategies for customer bid defense meetings or internal customers such as Therapeutic Strategy Leads, Medical Leads or business development.
- Collaborate with key stakeholders and IQVIA project teams to resolve issues.
- Prepare for planning meetings by conducting research into therapeutic areas using databases, scientific literature, the internet and expert medical knowledge.
- Be involved in 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.
- Proficient with planning tools, demonstrate a good 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 IT / Data Science OR Healthcare, Biological Science with sound IT/technical skills.
- Clinical/project management experience would be an asset as well as working knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.
- Effective communication, organizational and interpersonal skills.
- Advanced level of english is a must.
- Strong computer literacy, including well-developed computer skills in applicable software (SQL, Python) is ideal.
- Strong motivation and work ethic, can-do attitude.
- Ability to work independently and effectively prioritize tasks.