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Senior Site Budget & Contracts Lead (home based, Europe)

Aplica ya
Mapa de ubicación: Madrid, Spain Full time R1258690

Descripción del trabajo

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward.

The Site Budget & Contracts Lead is responsible for providing the suite of Site Budget & Contracts Services to clients. He/She will participate on a project team to deliver Site Budget & Contracts Services on time, within budget, and in accordance with applicable financial, contractual, and pharmaceutical R&D industry standards and regulations. Their focus will be on the more complex projects (i.e. multiple countries, challenging therapeutic area).

Responsibilities & Essential Functions:

  • Serve as the client’s primary point of contact for projects that are using a single Site Budget & Contracts service.

  • Lead internal project kick-off meetings for single solution engagements which will include a review of the Statement of Work (SoW) and the service delivery model that will be followed to execute the services.

  • Develop the investigator grant budget for the per patient grant and related site pass-through costs.

  • Work with the (Sr) Site Budget & Contracts Manager to develop site-specific Confidential Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), or other related contractual documents (collectively, the “contractual documents”) based upon client approved templates.

  • Negotiate contractual documents using the negotiation and escalation plan that has been established with the client.

Qualifications:

  • Bachelor's Degree preferably in a Business or Science/Health Care discipline, Nursing Degree, or equivalent degree and/or related experience.

  • Minimum of (5) five years of prior experience in a client service role at a biotechnology or pharmaceutical company, CRO, or other organization supporting clinical research or healthcare activities.

  • Clinical study start-up experience with an emphasis on site contractual documents.

  • Proficient with Microsoft Office, specifically MS-Excel and MS-Word.

  • Knowledge of the clinical trial process including GCP, ICH guidelines and relevant FDA/EC regulations/guidelines.

  • Multi-language skills are considered as a plus.

This position will be home-based in Europe. Preferred locations are Spain and France.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there!

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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