Senior Site Contract Associate - IQVIA Biotech

IQVIA LLC; Madrid; A distancia; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

IQVIA Biotech is seeking a Senior Site Contracts Associate for Spain, Portugal & Greece, homebased. You will support start-up contracting activities for selected sponsors, studies or multi-protocol programs, developing proposals and maintaining templates and systems.

Collaborate with sponsors, RSU regions and teams to deliver contracting scope on time and within project plans, ensuring regulatory compliance and high-quality contracting intelligence across the portfolio.

Formación

• Bachelor's degree in life sciences or healthcare with 6+ years in contract roles.
• Experience acting as a contract negotiator for sponsors or CROs.
• Knowledge of regulated clinical trial environment and drug development.
• Strong written and verbal communication; cross-functional collaboration.

Responsabilidades

• Support start-up contracting activities for sponsors, studies or programs.
• Prepare investigator grants estimates and proposal text; maintain templates.
• Ensure compliance with sponsor requirements and regulatory guidelines.
• Provide contracting support to enable study initiation and maintenance.
• Maintain CTMS, databases, timelines and project plans.

Conocimientos

Contract negotiations

Clinical site contracting

GCP/ICH knowledge

Regulatory understanding

Strong written communication

Team collaboration

Microsoft Office

CTMS familiarity

Educación

Bachelor's Degree in life sciences or health care

Herramientas

CTMS

Microsoft Office

Microsoft Outlook

Descripción del empleo

Senior Site Contracts Associate IQVIA Biotech Spain, Portugal & Greece - Homebased

Job Overview

Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities.

Essential Functions

Develop simple investigator grant estimates and proposal text to support the proposal development process. Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy. Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required. Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required. Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts, managers and directors as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.

Qualifications and Skills

Bachelor's Degree in life sciences or health care +6 years relevant experience, including demonstrable experience acting as a contract negotiator. Relevant sponsor or clinical research organization clinical site contracting experience. Good negotiating and communication skills. Good interpersonal skills and a strong team player. Strong technical writing skills. Understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards. Good organizational and planning skills. Strong knowledge of Microsoft Office and e-mail applications. Ability to interpret pricing models and to prepare proposals, bid grids and budgets. Good understanding of clinical trial contract management. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

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.