Study Grant Manager

IQVIA; Lisboa; Presencial; EUR 70 000 - 100 000; Tempo integral

Resumo da oferta

IQVIA is seeking a Study Grants / Clinical Trial Cost Expert in Lisbon to lead Grant Plan and FMV assessments for global and regional trials, IITs, and RCs. The role focuses on accurate budget forecasting and expediting site contracting while ensuring regulatory compliance.

The ideal candidate has life science education and strong budgeting experience, with proficiency in FMV concepts, GrantPlan and Grants Manager, and MS Office.

Qualificações

• Proven ability to exercise independent judgment, taking calculated risks when making decisions.
• Excellent communication and collaboration skills.
• Ability to work effectively in a global and cross-functional team environment.

Responsabilidades

• Lead Grant Plan & FMV assessments for Clinical Trials, IITs and RCs.
• Provide accurate cost estimations for budgeting and forecasting.
• Resolve FMV queries and ensure regulatory compliance in FMV/Grant Plans.
• Collaborate with Early Pricing Team to contribute to budget development.
• Maintain forecasting tools and ensure alignment with study objectives.

Conhecimentos

Independent judgment

Communication

Collaboration

Global cross-functional teamwork

Formação académica

BSc / MSc Life Science

Ferramentas

GrantPlan

Grants Manager

Pricing tools

Databases

Descrição da oferta de emprego

Lisbon, Portugal

Full time

R1562800

Position Overview:

The Study Grants / Clinical Trail Cost Expert is responsible for conducting Grant Plan and Fair Market Value (FMV) assessments for all Globally, Locally, and Regionally Supported Clinical Trials, Investigator Initiated Trials (IITs), and Research Collaborations (RCs). This role is integral in ensuring accurate budget forecasting and accelerating site contracting processes.

Accountabilities:

Grant Plan & Fair Market Value (FMV) Assessments :

• Lead the translation of clinical protocol assessments into Grant Plans and FMV cost estimations
• Develop FMV/Grant Plan Investigator Fees
• Resolve FMV queries
• Ensure compliance with regulatory guidelines and industry standards in determining FMV

Budget Forecasting:

• Provide accurate cost estimations, ensuring clinical operational and scientific requirements are reflected with accuracy
• Improve Grant Plan estimates and reduce need for revisions
• Identify cost savings utilizing cost data for estimations
• Collaborate with Early Pricing Team to contribute to overall budget development
• Maintaining accurate forecasting tools

Cross-functional collaboration:

• Collaborate with relevant teams to ensure alignment with study objectives and budget constraints
• collaborate with various leads to identify clinical/operational issues
• Partner closely with teams to improve trial forecast management
• Provide feedback on study protocol impacts

Qualifications:

• BSc / Msc degree in Life Science
• Knowledge and ability to apply ICH GCP and applicable regulatory guidelines
• Relevant sponsor or clinical research organization clinical experiencewith country-level or site-level budget development, including awareness of clinical trial contract management
• Experience with interpretation of clinical trials protocol assessments, budget negotiations
• Strong knowledge of Microsoft Office applications, pricing management tools and databases (e.g. GrantPlan, Grants Manager)
• Understanding of Fair Market Value concept and principles
• Knowledge of budget forecasting and financial analysis.
• Proven ability to exercise independent judgment, taking calculated risks when making decisions.
• Excellent communication and collaboration skills.
• Ability to work effectively in a global and cross-functional team environment.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com .

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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