Yale Center for Clinical Investigations is hiring a Clinical Research Analyst 2

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Yale Center for Clinical Investigations is hiring a Clinical Research Analyst 2.  This position reports to the Associate Director of Clinical Trial Resources in the Yale Center for Clinical Investigations (YCCI). YCCI has accountability for developing systems to manage clinical trials in all specialties throughout the University as well as in affiliated locations including Bridgeport Hospital. This position will develop the protocol builds in the OnCore clinical trials management system, to be followed by all clinical trial managers and teams across the University and affiliated locations. This position is responsible for accurate protocol build and management and reduction of compliance risk for human subject research at any/all of the following: YSM. YNHH, Yale-New Haven Saint Raphael’s, Yale-New Haven Bridgeport Hospital, NEMG, Yale-New Haven Greenwich Hospital and Yale West Campus. In addition, the industry Invoiceable research services are dependent on an accurate build.

Principal Responsibilities

1. Works closely with investigators and other study team members including the project manager, for projects or programs of a medium to large scope to consult, conduct analysis, and identify trial objectives and requirements.

2. Interprets research business needs and translates them into application and operational requirements. Develops necessary tools and workshops to successfully elicit requirements.

3. Critically evaluates information gathered from multiple sources – research protocols, clinical trial agreements, financial budgets and fees associated with research – to reconcile conflicts, and decompose high-level information into data essentials.

4. Receives and interprets requests for data extracts, analyses, and reports. Develops reporting modules, ad-hoc reports, and related reporting tools. Conducts research, data gathering, data analysis, modeling, projecting and scenario analyses, with the aid of planning technology and databases. Develops and harnesses the data that is available to identify existing business issues and key drivers and develops solutions and initiatives.

5. Analyzes data with standard statistical methods, interprets the results, and provides written summary and reporting of data analysis.

6. Develops, validates, deploys, implements, and maintains queries for the successful extraction of appropriate data.

7. Develops and maintain documentations and libraries on key processes.

8. Assesses risk and ensures compliance with research protocols/guidelines and university procedures.

9. Determines training needs, designs, develops and conducts training sessions, meetings and conference calls with study teams and staff members.

10. Collaborates with developers and subject matter experts to establish the technical vision and analyze tradeoffs between usability and business needs. Ensures strategic and tactical plans are carried out.

11. Communicates effectively the perspective of business opportunities, needs, and risks.

Required Education and Experience

  • Six to eight years of related work experience in the same job family and a Bachelor’s Degree in a related field; or an equivalent combination of education and experience.
  • Knowledge of research gained through experience working in a research setting as a project manager or other research team member.
  • Proven ability to understand research protocol and clinical trial agreements, and financial budgets and fees associated with the research with the ability to extrapolate relevant data to create the overall procedure and financial build for a clinical trial.
  • Strong systems skills required. Willing to obtain certification as an OnCore trainer.
  • Demonstrated ability to work independently and with a team. Proven ability to work as a project manager, business analyst or related position. Excellent organizational and analytic skills, with exceptional attention to detail and the proven ability to multi-task, trouble shoot and prioritize work.
  • Demonstrated knowledge regarding requirements for research involving human subjects.

Preferred Experience

Experience in the creation of research event schedules and schemas (calendars) as well as budget creation and milestones in OnCore or other comparable Clinical Trial Management System(s).

 

To apply, visit the Yale University website at http://www.yale.edu/hronline/careers/application/external/index.html

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