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.

Our hard-working teams combine and deliver centralized support and solutions for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the world to decrease startup timelines and go above and beyond.

This role is part of the global Site Payments team, which is dedicated to the processing of the Investigator Payments. As a Site Payment Associate, you will be dealing with one of the most complicated periods of the life-cycle of a clinical trial, which is essential part of our business operations and is a vital function within the Global Centralized Solutions group. By joining our diverse and dynamic team of professionals, you will have the opportunity to support key projects and gain insight on how the payment processes is performed within the clinical trial business.

A day in the Life:

Processing of investigator payments with strict adherence to contractual guidelines, country regulations and procedures. Overall responsibility to drive the payment generation process includes but are not limited to:

• Site Study Budget entry;
• Compile data from multiple sources to generate site payments based on completed patient activities and contracted milestones, as well as related pass throughs;
• Reviewing and processing of site invoices where required;
• Respond to and resolve payment-related issues and findings.
• Exhibit good financial stewardship in management of funds, investigator payments and project finances.
• Build and be a great partner with study sites and study teams.

Keys to Success:

Education and Experience

• Bachelor's degree or higher
• Previous experience in international corporate environment preferably with payments processing

Knowledge, Skills, Abilities

• Proficiency in English (verbal and written)
• Strong written & verbal communication skills; conflict resolution skills
• Self-organized person able to make decisions about daily tasks and priorities
• Ability to multitask and meet changing project needs whilst working in a fast-paced global environment
• Results driven with strong attention to details and ability to analyze project specific data
• IT literacy: MS Office, Clinical Trial Management Systems (CTMS), Financial Systems, etc.
• Good technical skills and ability to quickly learn new software

What we offer:

• Learning and development programme, ensuring you reach your potential
• Extensive benefits package based around the health and well- being of our employees
• Competitive salary
• Flexible working culture with work- life balance and possibility for remote working
• Collaborative and friendly environment
• Global exposure and opportunity to work on international assignments

Our 4i Values:

Integrity – Innovation – Intensity – Involvement

If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!