Are you a Data Analyst looking for a change? Large Pharma client has a need for a Data Analyst/Data Modeler with IDMP experience. Long term contract in NJ

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Data Quality Analyst Location: Princeton, NJ Duration: 12+ months initially with extension. Assists in the implementation of short- and long-term goals. Manipulates large data sets for quality and to ensure data integrity Understanding the relationships of objects and fields within RIM system to create, and run reports on a pre-set schedule. Executes work instructions to analyze large data sets and develop metrics Documents data quality metrics and creates compliance reports to upper management Responsible to review existing practices and propose updates based on changing regulations and trends. Actively participates in cross-functional sub teams to resolve complex issues. Demonstrates flexibility to work multitask and collaborate with other functional teams. Provides input in the review of the successes and failures of new approaches to capture lessons learned. Establishes and executes plans for managing workload within their assigned project(s) through efficient resource utilization and within designated timeframes. Effectively adjusts plans to deal with changes and obstacles. Thinks in a clear, decisive manner, remains calm under adverse conditions. Participates in personal development of self with supervisor by providing and asking for continuous and honest feedback. Enhance understanding of all the steps of the pharmaceutical drug lifecycle. Opportunity to manage multiple projects simultaneously and meet ambitious timelines. Work in diverse, multi-disciplinary teams to achieve business objectives. Understanding of key Research and Development projects and initiatives. Strengthen capability to operate in a fast-paced business environment with frequent challenges in change in direction and or shifting priorities. Refine attention to detail and develop critical thinking capabilities.

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Project Manager/Program Manager Location: Princeton, NJ Prepare and follow-up on Digital Health Steering Committee meeting Facilitate the preparation of monthly portfolio review materials (reviewing details and identifying highlights/trends to share) Analyze current portfolio of project in an EF sub-area to identify problems (e.g. PMs to fragmented or skills gap in financial tracking, inconstancy of completing status updates) and help formulate action plans to address Review the project schedules of existing projects to determine quality of the plans and identify potential risks\gaps Working with other directs to improve our PM process and experience

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IT Project Manager/Scrum Master Location: Princeton, NJ Project Manager/Scrum Master to drive Translational Medicine IT projects to successful delivery Responsibilities – IT Project Manager/Scrum Master Work with IT Business Partners and Technical Leads/Digital Capability Managers to deliver quality IT capabilities within Translational Medicine. Work with third party vendors and/or in-house developers, business/technical analysts, and QA resources to deliver key objectives of assigned projects while managing project scope, schedule, and cost. Act in the role of Project Manager and/or Scrum Master depending on methodology or approach chosen for a particular project. Act as a servant leader, removing impediments and other roadblocks on assigned projects. Track and manage project budget, ensuring accurate reporting of financials. Plan, measure, and track key performance indicators to ensure projects are delivered with quality. Facilitate project meetings and communications. Identify, document, and manage risks, issues, actions, and decisions and collaborate with project stakeholders to develop mitigation strategies as appropriate. Maintain project collaboration area (SharePoint, Jira, Confluence) and ensure completeness of documentation and appropriate access for required stakeholders. Regularly report project status to stakeholders, program management, and other IT leadership, prepare periodic status reports for project team, steering committees as defined through project governance. Identify resource needs and gaps in order to execute the project and operationalize the system into a support state. Oversee all QA and system validation activities to ensure compliance as required. Assist in executing a communication and change management strategy in support of project execution and rollout. Skills Required Minimum 5-7 years prior experience working in a Project Manager role and/or as a Scrum Master on large, complex IT projects. Experience in Biopharmaceutical Research & Development industry preferred Bachelor’s degree in computer science, engineering, physical sciences, or life sciences preferred Experience with formal Agile methodologies and SDLC practices Scrum and/or PMP certification a strong plus but not required Experience working with 3rd party vendors Strong proficiency in MS Project and other MS tools (Excel, Word, PowerPoint, Outlook) Experience using JIRA or other common Agile tools Lean Thinking / Six Sigma educated a plus Excellent oral and written communication skills; organizes and presents ideas in a convincing and compelling manner Exceptional interpersonal skills; able to communicate effectively with both technical and non-technical teams; able to provide technical leadership Outgoing personality; self-starter able to work interactively and independently with stakeholders

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Safety Business Analyst Location: Princeton, NJ Duration: 6+ months We are looking for a talented and passionate strategic Senior Business Analyst/Business Partner/Business Relationship Manager for our large pharmaceutical client to help with the strategic direction for information systems in Pharmacovigilance and Epidemiology area to ensure patient safety and compliance with global regulatory requirements This role will partner with other IT and PV functional groups to define, plan, prioritize, deliver & support information management capabilities. Specific Responsibilities Engages with PV business team to understand business strategies and translate them to multi-year digital capability roadmaps. Uses domain and technical knowledge to influence business strategies and align them with new digital capability opportunities. Develop and manage portfolio plans that Identify and prioritize digital capabilities that have the greatest impact on patient safety and product development Partners closely with IT Teams supporting clinical operations, regulatory and medical to ensure that cross-domain impacts and opportunities are identified and incorporated in to plans. Leads and facilitates process engineering activities based on practical knowledge of the broad range of systems and processes that support global pharmacovigilance and epidemiology sciences. Leads impact assessment of complex regulation changes across multiple domains or divisions Proactively researches industry and technology trends to inform strategic planning and translate to potential opportunities. Requirements Strong communication and relationship management skills Demonstrated ability to analyze business problems and identify technology solutions ( tactical solutions to operational issues and longer-term strategic planning). Develop business cases to demonstrate business value and develop appropriate implementation approaches for the solutions. Strong understanding of PV processes/regulations with focus on AE case collection and reporting Familiar with industry applications used for PV and case processing, ARGUS preferred 2-4 years of strong practical working experience with Pharmacovigilance and Epidemiology, with demonstrated command of processes and systems for adverse event collection, case processing, ICSR and aggregate reporting, signal detection and safety analytics. Experience with Argus, Empirica and E2B is preferred. Knowledge of new technologies for processing automation, digital AE collection and safety analytics is a plus. Demonstrated strategic leadership & track record of maintaining effective business relationships with Senior Management to ensure Informatics can deliver solutions that align with business strategies and objectives. Demonstrated experience with IT road map creation and portfolio planning. Proven abilities to plan, manage, and deliver strategic programs, from concept initiation through delivery. Demonstrated ability to conduct business analysis, requirements specifications and business change management. Experience in evaluating commercial products (e.g., software packages) and services and influencing the negotiation process for vendor products. Working knowledge of GxP regulations and delivery of informatics projects in a GxP environment. Must possess excellent written and verbal skills and demonstrate an ability to effectively communicate at all levels of the organization including executive stakeholders. Ability to achieve successful consensus among differing priorities and stakeholders in both the IT and Business communities. Effective in cross-functional, multi-site, matrix management and team building.

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