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Sunnyvale, California - USD Full Time Posted: Monday, 15 April 2019
 
 
Job Description

Project Manager to implement a Clinical Trial Management System (CTMS) in a Pharmaceutical R&D IT environment. Project management responsibilities include the coordination and completion of deliverables by each workstream on time, within budget and within scope. Oversee all aspects of the workstreams. Set deadlines, assign responsibilities and monitor and summarize progress of project. Prepare reports for upper management regarding status of project. Business Analyst duties include reviewing SDLC documentation.

The successful candidate will work directly with clients to ensure deliverables fall within the applicable scope and budget. He or she will coordinate with other departments to ensure all aspects of the project are aligned. In addition, the candidate will work as a liaison between client and vendor.

Responsibilities:

  • Coordinate internal resources and third parties/vendors for the flawless execution of the project workstreams
  • Ensure that all workstreams deliver on-time, within scope and within budget
  • Assist in the definition of project scope and objectives, involving all relevant stakeholders and ensuring technical feasibility
  • Ensure resource availability and allocation
  • Develop a detailed project plan to monitor and track progress
  • Manage changes to the project scope, project schedule and project costs using appropriate verification techniques
  • Measure project performance using appropriate tools and techniques
  • Report and escalate to management as needed
  • Manage the relationship with the client and all stakeholders
  • Establish and maintain relationships with third parties/vendors
  • Create and maintain comprehensive project documentation
  • Meet with clients to take detailed ordering briefs and clarify specific requirements of each project
  • Attend training as required to maintain proficiency

Requirements:

  • 1-5 years working experience in project management in a Pharmaceutical R&D IT environment
  • Knowledge of the Pharmaceutical Validation process
  • Knowledge of the SDLC process
  • Previous consulting experience
  • Excellent client-facing and internal communication skills
  • Excellent written and verbal communication skills
  • Solid organizational skills including attention to detail and multitasking skills
  • Strong working knowledge of Microsoft Office
  • Project Management Professional (PMP) is a plus
  • Working on projects with cloud computing is a plus
Company Description WriteResult's sister company 3C Company specializes in supporting the needs of the Global Pharmaceutical industry for software solutions. We partner with our clients to help them improve the speed, accuracy, and quality of their drug R&D capabilities. You can learn more about 3C Company at .

Sunnyvale, California, United States of America
IT
USD
WriteResult
WriteResult
JS59D423888/693973055
4/15/2019 8:05:35 PM

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