Senior Site Contract Associate

🔥 0 minutes ago

🌐 France, Greece, +2 more countries – Remote

🇫🇷 France – Remote 🇬🇷 Greece – Remote 🇵🇹 Portugal – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

✨ Associate

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Support delivery of required start-up contracting activities for selected sponsors, studies, or multi-protocol programs, including pre-award activities • Develop investigator grant estimates and proposal text to support proposal development • Maintain contract and budget templates, contracting systems, tools, processes, and training materials • Collaborate with sponsors, stakeholders, and RSU regions and countries to deliver project scope • Provide operational and financial contracting support for business development and clinical trial initiation and maintenance • Assist with creation and review of scientific, technical, and administrative documentation • Collect, interpret, analyze, and disseminate contracting intelligence • Ensure contracting efficiency and adherence to project timelines and financial goals • Report contracting performance metrics and out-of-scope contracting activities • Comply with contract management and quality standards • Provide administrative and operational support to investigator site contract analysts, managers, and directors • Maintain internal systems, databases, tracking tools, timelines, and project plans, with emphasis on CTMS

🎯 Requirements

• 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