Sr Analyst, Site Contracts

The Sr Analyst, Site Contracts is responsible for the preparation of clinical trial agreements, master clinical trial agreements, related ancillary services agreements and amendment templates as well as the negotiation of language, budgets, and payment terms with clinical sites and ancillary facilities. The Sr Analyst, Site Contracts supports the achievement of study site activation goals, as well as ensuring contracts are amended in a timely manner throughout the lifecycle of studies. Prepare appropriate contract templates, building on previous negotiations with institutions to speed and streamline negotiations. Work closely with study and legal teams to ensure start up timelines are met, contract terms meet study needs and protect Biogen’s interests, and good site relationships are maintained. Manage status tracking and reporting from draft preparation to full execution, and ensure Biogen is always inspection and audit ready. Serve as an escalation point for language escalations from external entities, as necessary. Analyze contract trends, identify and support process improvements, and assist with developing and refining institutional knowledge repositories and negotiation parameters; provide mentoring and support to site contracts analysts.