Project Lead – Project Manager

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🕒 2 days ago

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• The Project Manager serves as the Project Lead and primary sponsor contact and is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. • Additionally, the Project Manager establishes and communicates customer expectations to the project team and ensures that escalation pathways are adhered to internally and externally. • The role involves leading the cross functional project team to meet or exceed deliverables. • Responsible for the delivery of the cross-functional project (time, cost, quality)​ by working closely with Global trial and functional leads. • Ensures escalation pathways adhered to internally and externally. • Ensures financial stewardship at a trial level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out-of-Scope activity, drive the Con Mod process/negotiations and team execution to timelines. • Establishes, communicates and manages customer expectations to achieve optimal delivery during the project. • Drives Risk Identification and Issue Resolution at project level. • Ensures project team compliance with organization policies, SOPs, ICH-GCP, regulatory and project specific requirements. • Responsible for vendor management, where required.

🎯 Requirements

• B.A. or B. Sc. in a scientific discipline. • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years) with 2+ years of project/trial management. • Related scientific and clinical expertise and exceptional project-management, risk-assessment, contingency-planning, and communication skills. • Extensive knowledge of clinical development related to one or more trial phases (I, II, III), as well as cross-functional drug development. • Expertise in Good Clinical Practices (GCP), International Council for Harmonization (ICH) guidelines and regulatory requirements for clinical development. • Ability to establish and execute operational plans. • Technical and systems competency, such as computer skills, to include effective use of systems and applications such as Microsoft Outlook, Word, Excel and PowerPoint, as well as organization systems. • Ability to delegate and effectively prioritize own and workload of project team members in a frequently changing environment. • Effective oral and written communication and presentation skills.

🏖️ Benefits

• Health insurance • Paid time off • Flexible working arrangements • Professional development opportunities