Description
We are seeking a Clinical Research Coordinator to provide input into the generation of study strategies and collaborate with other IQVIA teams. You will perform, manage, and coordinate activities for assigned opportunities/projects, including data mining, desk research, and literature analysis, and formulate recommendations to present to internal and external stakeholders.
Essential Functions
- Conduct desk research and literature review analysis for data source characterization
- Make recommendations for IQVIA commitments of future studies by delivering accurate and robust data source landscaping, country, site or enrollment strategies
- Support the development of materials related to feasibility or site lists or enrollment strategies for customer bid defense meetings or internal customers
- 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
- Present results of data gathering and analysis activities
- Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research
- Demonstrate proficiency with planning tools and understanding of system features and functions
Qualifications
- Bachelor's Degree in Healthcare or Biological Science
- 1 year of relevant experience in clinical research
- Clinical/project management experience is preferred
- General knowledge and understanding of company clinical systems, procedures, and corporate standards
- Working knowledge of medical terminology, GCP, FDA regulations, and Drug Development process
- Sound understanding of clinical research
- Effective communication, organizational, and interpersonal skills
- Strong computer literacy, including well-developed computer skills in applicable software
- Ability to work independently and effectively prioritize tasks
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