Clinical Trial Coordinator II

Job not on LinkedIn

🕒 May 26

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

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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

• Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation. • Independently perform tasks related to planning, and execution of clinical studies. • Support critical day-to-day clinical study activities, including regulatory inspection readiness. • Collaborate with Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs). • Review and/or approval of study documentation. • Supporting oversight of risk-based monitoring. • Attendance of key team meetings as required; may make presentations. • Supporting regulatory inspection readiness. • Support clinical trial systems (e.g. CTMS/TMF). • Support study close-out activities.

🎯 Requirements

• Bachelor’s degree or equivalent international degree required. • 2-4 years’ experience in pharmaceutical industry, clinical research organization, or related role. • Experience in Phase 2 and 3 studies and global/international studies is advantageous. • Experience working across multiple therapeutic areas (including oncology) is advantageous. • Experience in the study start up field. • Knowledge in global/regional regulatory and compliance requirements for clinical research. • Demonstrated excellence in task management and cross-functional collaboration. • Excellent communication skills. • Fluent business English (oral and written).

🏖️ Benefits

• Health insurance • 401(k) matching • Paid time off • Flexible work arrangements • Professional development opportunities