
Biotechnology • Pharmaceuticals • Healthcare Insurance
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Yesterday

Biotechnology • Pharmaceuticals • Healthcare Insurance
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
• The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. • Communicate with project team members regarding study updates. • Maintain documentation as required by protocols, SOPs and regulatory standards. • Provide systems support and track information related to the status of study activities. • Assist with general administrative functions as required. • Document and track study activities using relevant forms and tools. • Assist in the preparation of study and site-specific materials in accordance with relevant SOPs. • Complete minute taking and documentation for sponsor/external or internal teleconferences as requested. • Provide support to project team including proof-reading and editing correspondence, assembling study documents, and arranging meetings.
• Diploma – Associate degree or equivalent. • 2-3+ years of relevant Clinical Research experience in pharmaceutical or CRO industries may be considered. • Good oral and written communication skills. • Proven leadership within the CTA group. • Good organizational and time management skills. • Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint). • Critical Thinking and Problem Solving. • Language Skills Required: Speaking: English and local language. Writing/Reading: English and local language.
• Medical • Dental • Vision • Life • STD/LTD • 401(K) • ESPP • Paid time off (PTO) or Flexible time off (FTO) • Company bonus where applicable
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