Trial Feasibility Specialist

at  Thermo Fisher Scientific

JOB DESCRIPTION

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

• Coordinates global site identification assessments and provides updates to all global participants as required.
• Coordinates programming and validation of feasibility surveys according to the timeline, quality standards and client expectations.
• Provides matrix management of internal team members in site identification assessments, identification of risks and development of mitigation plans.
• Prepares global site identification data analysis and formal progress reports (including narratives) within established timelines.
• Participates in alternative clinical intelligence gathering initiatives as alternatives to survey drive site identification assessment.
• Responds accurately to department email and telephone inquiries from internal and external clients.
• Assists with additional department objectives and projects as necessar