Global Investigator Site Payments Lead

Job description

Nombre del sítio: Canada - Ontario - Mississauga, Greater Poland, GSK House, Stevenage
Fecha de publicación: Jan 24 2024

Job Purpose:

The Global Investigator Site Payments Lead is a key role within the Global Site Budgets & Contracts (GSBC) team responsible for driving upper quartile performance by overseeing key processes relating to accurate and timely payments to investigator sites in line with protocol requirements and study specific contracts. This role will provide functional expertise in the development of study specific Subject Visit Template (SVT) or equivalent, data acquisition and investigator site payment procedures/systems. The GSBC team will function as a global Centre of Excellence for the entire end-to-end process (i.e., from protocol development to study conclusion), providing an integrated, consistent approach to benchmarking, site budget development, contracting, SVT development and payments.

Key Responsibilities:

The responsibilities of this role include but are not limited to the following:
• Lead the internal process for SVT development and payment data acquisition
• Working with other members of the GSBC team to prepare study-specific visit definitions to ensure visit payments are structured to allow for proper and efficient payment of study visits, considering any conditional elements of the study design
• Serve as POC for country study team and SDLs on SVT and payment process issues; identify and proactively raise issues and concerns in a timely, open, and appropriate manner
• Drive continuous improvement in site payment processes, including assessment and implementation of new system/tools
• Act as expert to assist global study teams in developing a study-specific Subject Visit Template (SVT) to optimally facilitate the feed of clinical data to the operational systems landscape for the combined purposes of enrollment tracking, visit tracking and investigator payments
• Develop and maintain global guidance, process maps, templates, and training for the creation of Subject Visit Templates
• Actively engage organizations and country representatives on global standards and process and communicate changes
• Identify issues which consistently appear for same study types, study design scenarios, complex study designs (cohorts/arms/sub-studies), payment scenarios, subject enrollment tracking, mapping feed and user acceptance testing and drive adoption of global standards to mitigate issues and simplify processes
• As Subject Matter Expert, participate in related system projects/workstreams and development of business requirements

• May oversee service provider

Why You?
Basic qualification:

3 years or more of relevant experience with investigator payments process and governance in the Pharmaceutical, Biotech Clinical R&D industry. Bachelor’s degree in business, Science, Math, or related discipline.
Preferred Qualifications: In addition to the basic qualification, experience in Pharmaceutical, Biotech with an emphasis on operational data acquisition/management process and systems landscape within a clinical research/drug development environment.

Job-Related Experience/ Skills / Background:
• Knowledge of investigator site payment requirements and experience operationalizing timely and accurate payments to sites.
• Demonstrated high degree of understanding of clinical data, clinical and data management processes, ability to interpret protocol design to optimally represent the study and address multiple operational processes
• Operational knowledge of clinical research and understanding of R&D and drug/vaccine development process.
• Experience with User Acceptance Testing
• Ability to influence global contributors/study teams and drive agreement with regards to broad-based operational requirements
• Knowledge of industry payment technology and tools
• Strong business acumen, planning, negotiation, and organizational skills
• Demonstrated track record in quality decision-making and problem resolution that impacts study/program direction. Recognizing potential risks and can implement effective mitigation strategies.
• Proven ability to work effectively in a highly matrixed environment with internal and external customers based locally, regionally and globally.
• Good networking skills with internal and external partners and contacts within other GSK business units
• Confidence in working in an environment that is constantly evolving with new processes, tools, and systems, internally and externally. Understands and effectively utilizes change management tools and approaches.
• Independent and proactive with experience with internal and external team stakeholders to drive process improvement initiatives and implement solutions
• Good understanding of medical terminology and procedural, material, and administrative costs associated with the site work performed in clinical trials.
• Fluent written and verbal communication skills are required in English.

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