Site Contracts Manager

🕒 il y a 1 jour

🌐 Espagne, Pologne, +4 autres pays – Distant

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⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

👔 Manager

👻 Score fantôme 10%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Precision For Medicine

Precision For Medicine

1001 - 5000 employés

🏥 Santé

💼 Conseil

📦 Logistique

💰 €75 000 000 Private Equity Round en 2015-12

Healthcare • Consulting • Logistics

Precision for Medicine est un leader spécialisé dans l’accompagnement du développement et de la mise sur le marché de thérapies innovantes, notamment en oncologie, dans les maladies rares et les maladies auto-immunes. Grâce à une gamme complète de services — gestion d’essais cliniques, services de laboratoire et collecte de biospécimens — l’entreprise intègre des capacités avancées en biomarqueurs ainsi que des solutions de fabrication pour fluidifier des processus de développement clinique complexes. Sa mission est d’accélérer la recherche et d’apporter aux patients des solutions médicales qui changent la vie, en dépassant les inefficacités traditionnelles souvent observées dans le paysage du développement pharmaceutique.

Description

• Review, draft, negotiate and track confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements • Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts • Work with supervisors and internal/external stakeholders to resolve or escalate contractual issues • Ensure adherence to company policies, procedures and contracting standards • Update study team members on contract negotiation and execution status • Establish, track, report and manage site contract metrics • Support maintenance and archiving of contract files and databases • Assist in designing and implementing procedures for timely contract execution • Identify process improvements and take corrective action • Perform other assigned tasks

🎯 Exigences

• Graduate, postgraduate, 4-year college degree • Experience in a CRO/healthcare field • At least 5 years’ experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations • Experience leading interactions with Study Teams and Sponsors • Preferred: Bachelor's in law, scientific fields, business administration or equivalent degree • Preferred: Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations • Proficiency in MS Office software programs and computer applications • Ability to handle sensitive issues with discretion • Ability to work independently and cooperatively in a virtual environment

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