Global Investigator Site Payments Lead - Middlesex, United Kingdom - GSK

GSK

Verified Company

Middlesex, United Kingdom

4 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Site Name:
Canada - Ontario - Mississauga, Greater Poland, GSK House, Stevenage

Posted Date:
Jan

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 studyspecific 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 studyspecific 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
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 broadbased operational requirements
Knowledge of industry payment technology and tools
Strong business acumen, planning, negotiation, and organizational skills
Demonstrated track record in quality decisionmaking 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.

LI-GSK

Why Us?

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive.

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