**Job Overview:** The Clinical Plan and Analysis Data Scientist will perform, manage and co-ordinate activities for complex opportunities/projects. They will utilize multiple data sources to perform analysis, formulate recommendations and present to internal and external stakeholders. They will also train, and mentor junior staff and country leads and make recommendations and lead process improvements. **Essential Job Functions, Duties and Responsibilities:** • 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. **Knowledge, Skills, and Abilities:** • 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 applica ble software. Python & SQL programming experience required. • Ability to work independently and effectively prioritize tasks. **Qualifications:** • Bachelor’s degree in healthcare, Biological Science, Computer Science, or Statistics Required; Master’s or higher degree preferred. • Minimum 5 years’ related experience in clinical research. Equivalent combination of education, training, and experience. **\#LI-Remote** IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled