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Job Title: Clinical Business Analyst
Location: Onsite- East Coast hours
Duration: 6 Months

About the Job:
Our client is looking for a Clinical Business Analyst who will be the vital link in supporting and ensuring the successful implementation of Veeva Clinical Operations Vault. You should have a strong analytical background in Pharma, including building, testing, and deployment tasks.


Responsibilities:
  • Assist Customer Support and Account Management leadership with identifying patterns and relationships in data; produce periodic and ad hoc reports based on these analyses.
  • Produce and improve the existing reporting model to provide repetitive and regular analytics to the business leaders.
  • Partner with business teams to define and prioritize reporting system enhancement requests.
  • Identify and optimize the true drivers of financial performance, productivity, customer engagement and other metrics that support the business.
  • Capture the strategic, operational, and tactical business process goals and objectives.
  • Employ critical metrics and KPIs that drive success and design reporting solutions to measure organizational performance.
  • Research best practices to support developing solutions and recommendations for current business operations


Minimum Job Qualifications
Project Planning, Management, and Oversight: Develop project plans and manage timelines to ensure Clinical contributions to the initiative are met. Draft core team meeting agendas and ensure meeting outcomes are captured. Contribute to management presentations to highlight scope, timeline, risks, and mitigation steps related to major releases as well as the outlook for future application roadmap.

System Specifications: Participate in workshops and sprint team meetings designed to align on and document application requirements. Translate requirements into use cases that describe how the functionality will be used on a daily basis within the organization. Advocate for high-priority needs on behalf of end users in a positive, solution-oriented way.

Process Flows: In parallel with developing system specifications, determine how the deployment of system functionality affects existing business processes including the timing and quality of key data

Reporting: Interface with the core team and end-users to ensure that standard reports within the applications are specified, tested, and functioning to enable timely operational oversight, informed decision-making, and enable a culture of continuous improvement.

System Design & Configuration: Interface with the technical development team to ensure that specifications are documented at an appropriate level of detail and understood. Clarify any ambiguous requirements with users on behalf of the technical team and reflect refinements in the documentation. Lead review of any initial prototypes on behalf of the Client. Document feedback on prototypes vs requirements as applicable. Advocate for end users to ensure high-priority requirements are met.

System Testing and Release: Provide input to the testing plan to ensure that applications are functioning according to documented system specifications including "scripts” or scenarios for users to test. Document whether the application meets desired requirements or not including explanation and prioritization of any gaps. Partner with the core team on the clear go/no go criteria for system release to production.

Training: Provide input to training and change management plan, including review of material to be used in implementing and supporting new applications/functionality. Aid in the coordination of training sessions for specific user roles/functionality across locations to ensure end-users are adequately trained.

Desk-side support: As part of a support network, including local system subject matter experts, provide desk-side support to answer user questions, direct users to appropriate training material and log/prioritize system "bugs” with the technical team for remediation Communication Plan: Develop a communication plan using a variety of means including email, presentations at global/local meetings, posting to MSTeams sites to keep stakeholders informed of the outlook for clinical trial management and near-term activities to support design and implementation.

Education:
  • Bachelor's degree or technical certificate in mathematics, statistics, data analysis, computer science, or a related field.
  • Or, any combination of education and experience which would provide the required equivalent qualifications for the position.

Professional Requirement:
  • 5 years experience in the pharmaceutical industry supporting clinical development
  • In-depth experience within various aspects of the system design lifecycle including the application of agile development methods
  • Experience with Benchling for Clinical Trial Management
  • Experience with configuration and use of Veeva Clinical Operations Vault including TMF, SSU, and CTMS modules. Ideally, experience with cross Vault integrations such as between Regulatory RIM and/or Safety and the Clinical Operations Vault
  • Leadership skills to collaboratively interact with and influence stakeholders at all levels of the organization in a multi-disciplinary team, global environment
  • Excellent project management, planning, and organizational skills. PM certification is a plus.

Last updated on Feb 8, 2023

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