RWE Senior Site Strategy Lead
IQVIA
Summary
The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for proposal.
Job description
Job Overview
The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for proposal.
The SSL is key in building the most efficient and effective scenario for study execution during our sales process. This global team is working closely with other functional unit leads, and having the ability to build a strong proposal that IQVIA is able to operationalize and execute.
In addition to the pre-award support the team provides, the SSL is very involved in the post award phase early on, and will work with the assigned Clinical Operations Lead (COL) to ensure that the sold Data Generation strategy is passed on to the assigned study team.
Key Activities
- Assist with overall project efficiency and adherence to project timelines and financial goals.
- Assist with turning a study budget and strategy into action that make RWE studies more predictable, shorten timelines, improve data quality and provide innovative solutions to the clients.
- Act as a single functional lead for Data Generation proposals, covering Site ID, Site and Patient Engagement, Site Management and Technology strategies.
- Partners with internal teams to understand relevant challenges within a study and to identify the Data Generation strategies that can help meet these challenges.
- Serves as single point of contact on the study to answer pre and post award site strategy questions.
Qualifications
- Prior experience and knowledge of clinical operations – monitoring processes, documentation, GCP standards
- In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of project budgets and the use of pricing tools.
- Strong analytical skills with ability to dissect budgets, negotiate prices with internal teams and understand the “big budget picture”.
- Strong verbal and written communication skills
- Results-driven with focus on excellence and quality.
- Excellent time management skills, ability to manage several projects with overlapping deliverables & schedule.
- Strong team player and collaborator with ability to operate in fast-paced environment.
Requirements
- Prior experience and knowledge of clinical operations – monitoring processes, documentation, GCP standards
- In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge of project budgets and the use of pricing tools
- Strong analytical skills with ability to dissect budgets, negotiate prices with internal teams and understand the “big budget picture”
- Strong verbal and written communication skills
- Results-driven with focus on excellence and quality
- Excellent time management skills, ability to manage several projects with overlapping deliverables & schedule
- Strong team player and collaborator with ability to operate in fast-paced environment
Benefits
- Health and welfare benefits
- Incentive plans
- Bonuses
Company overview
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Headquartered in Durham, North Carolina, the company operates in over 100 countries with approximately 86,000 employees worldwide. IQVIA specializes in creating intelligent connections across all aspects of healthcare through its proprietary IQVIA Connected Intelligence platform, which combines analytics, transformative technology, big data resources, and extensive domain expertise. The company's comprehensive portfolio includes clinical trial management, real-world evidence generation, commercial insights, and regulatory compliance services. IQVIA serves a diverse client base including pharmaceutical manufacturers, biotechnology companies, medical device firms, government agencies, and healthcare providers. With its Healthcare-grade AI capabilities and extensive global data assets, IQVIA accelerates the development and commercialization of innovative medical treatments while improving healthcare outcomes for patients globally. The company is publicly traded on the New York Stock Exchange under the ticker symbol IQV.