Thermo Fisher Scientific
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.
Clinical Trial Manager – Cardiovascular, General Medicine
Job not on LinkedIn
November 7
Thermo Fisher Scientific
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
• Direct, coordinate, and manage technical and operational aspects of projects • Ensure successful completion of clinical trials within agreed timelines and budget • Lead clinical operational and quality aspects of allocated studies • Collaborate with project manager and clinical management team • Develop clinical tools and maintain documentation • Regularly communicate with the clinical team and lead meetings • Monitor clinical trials to assess performance and ensure compliance • Prepare and review clinical activity timelines and provide updates • Coordinate start-up activities and ensure document quality
🎯 Requirements
• Bachelor's degree or equivalent • Previous experience comparable to 5+ years • Strong leadership skills and effective mentoring • Strong planning and interpersonal skills • Solid understanding of change management principles • Comprehensive understanding of clinical monitoring practices • Strong judgment, decision making, and risk leadership skills • Effective oral and written communication skills in English • Strong financial competence and knowledge of budgeting • Strong computer skills with office applications • Ability to independently handle clinical studies
🏖️ Benefits
• Reasonable accommodation for individuals with disabilities • Health insurance • 401(k) matching • Flexible work arrangements • Professional development opportunities • Paid time off
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