Clinical Trial Operations Specialist
hace 2 semanas
Job Overview
We are seeking a highly skilled Clinical Trial Operations Specialist to join our team at Thermo Fisher Scientific. As a key member of our Global Study Team, you will contribute to the successful delivery of clinical studies by overseeing operational activities from study set up to archival.
Responsibilities
- Oversee the setup and maintenance of internal systems, databases, and tracking tools to ensure study completeness and inspection readiness.
- Work closely with the Study Manager or Study Delivery Lead to manage end-to-end operational study delivery activities.
- Collaborate with internal and external partners to drive continuous improvement initiatives and share best practices across business units.
- Maintain interactions and meetings with internal and external stakeholders to ensure study success.
- Manage vendor relationships and oversee the delivery of clinical supplies, investigational products, and study materials.
- Ensure data quality and oversight to guarantee study inspection readiness.
- Contribute to squad activities as per STOM requirements.
Requirements
- Graduate/Bachelor's degree in life sciences or related field.
- At least 1+ years of relevant work experience in a pharmaceutical/scientific environment.
- Scientific background and knowledge of clinical trials (including ICH-GCP) and drug development process is an asset.
- Familiarity with key systems used in clinical trial delivery.
- Strong project management skills with analytical/financial skills.
- Excellent verbal and written communication in English.
- Ability to manage multiple competing priorities with good planning, time management, and prioritization skills.
What We Offer
- Opportunity to contribute to life-changing therapies.
- Comprehensive training and development programs.
- A collaborative and inclusive work environment.
- Attractive compensation and comprehensive perks.
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