Sr Project Manager - Labs (Biopharmaceuticals) at PPD in Middleton, WIother related Employment listings - Middleton, WI at Geebo

Sr Project Manager - Labs (Biopharmaceuticals) at PPD in Middleton, WI

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health. Envision a workplace where you have a direct impact on improving health, work alongside expert scientists, use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success. As a Senior Project Manager you are responsible for direct oversight of client project portfolio management. The Senior Project Manager provides leadership of the PPD project team and acts as chief liaison to the operational personnel of major clients, often working globally, with multi-functional leads to appraise project risks, interpret data, apply financial stewardship and achieve timely and high quality study milestones. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.
Essential Functions:
Provides oversight and coordination of client portfolios. Provides oversight to internal departments and external clients to ensure the project requirements are understood, agreed and followed at all times (requires negotiating and real-time decision making with clients). Facilitates the flow of technical and laboratory information to all stakeholders. Consults and uses, where appropriate, the scientific input of laboratory management and technical staff to assist the client with management of the project. Prepares the project specifications documents and follows the preparation according to budgets and contracts. Maintains at all times an updated project master file with version controls for specs, budgets and contracts. Ensures sponsors have authorized and signed off most recent versions of all documents and that a contract exists prior to deliver any services. Assures compliance with FDA and Good Manufacturing Practice guidelines, PPD SOP's, personnel policies and procedures, PPD Exposure Control Plan, IATA, and other regulations regarding the transport of biological specimens. During initial review of project documentation, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent project documentation amendments. Obtains other functions' commitment to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD internal departments performing the required tasks during all project phases. Controls, manages and follows day to day activities during the course of the project to resolve any issues and answer queries. Actively consults with IT and data management development groups in the design, validation and implementation of new software and functionalities pertinent to project management activities. Consults with BD and finance staff during initial project documentation review on standard services and costs, supporting RFP feasibility assessments. Advises on possible solutions if needed. Drafts responses for proposals. Responsible for accurate invoicing and coordinates with Finance and laboratory management for all billing/invoicing for the client's portfolio of projects. #LI-TH1
Salary Range:
$80K -- $100K
Minimum Qualification
Business Project Management, Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications.

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