Senior Process Optimization Specialist, Clinical Research Group

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🕒 March 23

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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

• Proactively collaborate with initiative leads and management to prepare, organize, coordinate, document and/or provide the development and delivery of department products and services to a globally dispersed, cross-functional audience in support of business outcomes and industry compliance requirements. • Develop varied support materials, presentations, and/or tools to support department's remit and strategies. • Proactively collaborate with initiative leads and management to develop, optimize and improve processes, associated systems/applications, training and communications. • Lead small to medium-scale process improvement initiatives. • Develop process improvement processes and solutions. • Identify and collate information required to assess compliance with processes and to prioritize business process improvement needs. • May review, assess and update procedural documents for overall compliance with current processes. • Perform special projects, assignments and administrative tasks per business needs. • Provide training and guidance to junior team members

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). • Significant clinical research experience in all phases of clinical study life cycle, including start-up, interim and close-out, is preferred. • Thorough understanding of procedural documents • Strong understanding of process improvement fundamentals • Solid investigative and analytical skills • Strong negotiation skills • Thorough understanding of clinical management technology and systems, and strong computer skills • Effective judgment, decision making, escalation, and risk management skills • Effective oral and written communication skills including the ability to communicate in English, both orally and in writing • Strong interpersonal skills and problem solving ability • Capable of directing and promoting teamwork in a multi-disciplinary and/or multi-cultural team setting • Strong attention to detail • Thorough understanding of regulatory guidelines and directives • Strong creative and critical thinking skills

🏖️ Benefits

• Health benefits • Paid time off • Flexible work arrangements • Professional development opportunities