Thermo Fisher Scientific
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.
Clinical Trial Coordinator II
Job not on LinkedIn
🕒 May 26
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Thermo Fisher Scientific
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
• Coordinates, oversees and completes functions on assigned trial(s) activities • Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system(s) • Ensures allocated tasks are performed on time, within budget and to a high quality standard • Proactively communicates any risks to project leads and line manager as appropriate • Performs administrative tasks on assigned trials including timely processing of documents, performing (e)TMF reviews, distributing mass mailings and communications as needed • Reviews and tracks local regulatory documents • Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials • Ensures that trial status information relating to activities is accurately maintained in the database and current at all times • May develop and maintain relationships with client local affiliates and support the maintenance of study specific documentation
🎯 Requirements
• High / Secondary school diploma or equivalent • Bachelor's degree preferred • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years) • Ability to work in a team or independently, as required • Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively • Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency • Strong customer focus • Demonstrated flexibility and adaptability to reprioritize workload to provide efficient support • Excellent English language and grammar skills and proficient local language skills as needed • Excellent computer skills, proficient in MS Office (Word, Excel, PowerPoint) and ability to obtain knowledge and master relevant systems
🏖️ Benefits
• Comprehensive health insurance • Retirement plan options • Paid time off • Flexible work arrangements • Professional development opportunities
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