The Associate Design Analytics Lead defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making. This an individual contributor role.
Job Overview
Perform, manage and co-ordinate activities for assigned opportunities/ projects. Utilize multiple data sources to perform analysis, develop data storyboards, collaborate internally to formulate meaningful client insights and reports, and present to internal and potentially external stakeholders. Train and support new team members / junior staff. Make recommendations for process improvements and contributes to innovation.
Responsibilities
- The Associate Design Analytics Lead defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making. This an individual contributor role.
- Conduct and delivery of Protocol Assessments as part of new opportunity development and on-going project delivery. Responsibilities include working with sales, Medical and therapeutic strategy leads, and global feasibility leads and other stakeholders to understand key challenges within a protocol design, identifying and executing standard and custom analytics to pressure test protocols, and interpreting and summarizing the findings from those analytics into meaningful insights.
- Ensure quality and timely project deliverables
- Partner cross functionally to present protocol assessment findings and to determine collaboratively how to apply the results
- Ensure all relevant data is leveraged for and included in client deliverables
- Make recommendations and suggestions to the team regarding data utilization and process implementation
- Coordinate the collection and delivery of appropriate data and analytics from broad range of sources to address trial design related questions
- Reconcile and interpret cross-functional data
- Function as a subject matter expert for data sources and tools utilized within the protocol assessment process
- Input into, review, and production of proposal text
- Contribute to training and support of new team members
- Participate in the continuous improvement of departmental processes and procedures
- May participate in functional area initiatives, special project assignments and act as departmental cross functional liaison.
- Maintain proficiency of skills and knowledge and remain current with industry trends based on current literature
- Typically requires 3 - 5 years of relevant experience in clinical research. Equivalent combination of education, training and experience.
- Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.
- Bachelor's Degree Healthcare or Biological Science
- Clinical and/or data analytics and/or consultative experience
- 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.
- Fluent English
- Strong computer literacy, including well-developed computer skills in applicable software.
- Ability to work independently and effectively prioritize tasks.
- Occasional travel.
