Remote, Monza e Brianza, Bulgaria
13 days ago
Sr Site Payments Associate FSP

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 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 goal-driven 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 exceed expectations.

This role is part of the Functional Service Partnerships (FSP) Site Payments team, which is dedicated to the processing of the Investigator Payments. As a Site Payment Associate II, 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 Integrated Clinical 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.

Discover Impactful Work:

Provides senior administrative, reporting, contractual and financial support to the department related to the processing of payments to investigative sites. Responsibilities include data compilation, issue/risk resolution, ensuring adherence to contractual guidelines and country regulations, and providing training and guidance to junior team members. Compile data from multiple sources to generate payments to sites in accordance with procedural documents and site contracts.

A day in the Life:Ensures adherence to country-specific regulations which affect and impact ability to pay. Manages payment responsibilities and workflow to meet contracted timelines and project deliverables.Builds and leads relationships with study sites and interface, on occasion, with clients for payment-specific issues.Responds to study-related escalations and resolves payment-related findings. Raises project risks appropriately.Trains study teams on site payment processes, including setting expectations around site payments' requirements and deliverables.May process investigator payments in middleware and financial system; manage refunds, credit notes, late payment fees, pre-payments or investigator meeting reimbursements.May build and enter budgets and SVTs; work on transparency reporting; perform study reconciliations; lead and maintain investigator funds tracker for studies transitioned to site payments.As a senior team member, assists in providing training, guidance, and review to junior team members.Keys to Success:EducationHigh / Secondary school diploma or equivalent and relevant formal academic / vocational qualification / Bachelor's degree preferred Technical positions may require a certificate.ExperiencePrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years).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, AbilitiesStrong organizational skills and strong attention to detailProven ability to handle multiple timeline sensitive tasks efficiently and effectivelyFlexible and able to reprioritize workload to meet changing project needsStrong computer skills, proficient in MS Word and Excel; preferred experience using CTMS, EDC, or financial systemsCapable of working independently and as a team member, promoting strong team approach and serving as a role model to othersEffective communication skills, which includes English language (oral, written) and other languages would be an advantage (where applicable)Demonstrated ability to extract pertinent information from study documentation such as protocol, contracts, budgets, etc. and perform applicable data entry of said documentsStrong ability to effectively analyze project specific data/systems to ensure accuracy and efficiencyGood understanding of ICH Good Clinical Practices, Country Regulatory and/or applicable tax regulations, etc. for all nonclinical/clinical aspects of project implementation, execution, and closeoutCapable of mentoring and training junior team membersDemonstrated ability to effectively analyze project specific data/systems to ensure accuracy and efficiencyWorking Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.Able to work upright and stationary for typical working hours.Ability to use and learn standard office equipment and technology with proficiency.Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.May require travel. (Recruiter will provide more details.)

Demonstrated ability to effectively analyze project specific data/systems to ensure accuracy and efficiency

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