Associate Trade Compliance Manager

Job description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 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! We have a vacancy for an Associate Trade Compliance Manage r in our Global Clinical Supplies Team. The role can be fully home-based. A day in life: Support developing Trade Compliance Import/Export strategy for studies. Support ensuring studies are always in compliance with Trade Compliance, local regulations, company requirements and client needs. Develop proficient communication and interaction with internal and external stakeholders to coordinate efforts, provide recommendations, and issue alerts to avoid obstacles during the import/export processes. Develop Trade Compliance Import/Export strategy and serve as the primary point of contact and escalation for Trade Compliance and Import/Export matters for low complexity assigned studies. Stay up to date with new processes and regulations concerning Trade Compliance and Import/Export. Support process improvement initiatives. Keys to success: Education and Experience: Bachelor's degree or equivalent and relevant formal academic/vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). Prior experience in clinical research, specifically in clinical supplies import/export, is preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: Good understanding of import/export operations, local and global regulations and clinical trial supply operations Good interpersonal, planning, organizational, problem-solving and decision-making skills Good understanding of the Microsoft Office suite Good focus on customers and attention to detail Ability to work as team, as well as work independently with substantial mentorship Fluency in English (reading, writing and speaking)