Clinical Trial Agreement (CTA) Management (Madison, WI)

Clinical Trial Agreement (CTA) Management

jobs(at)globalchannelmanagement.comClinical Trial Agreement (CTA) Management needs 3-5 years of experience creating negotiating and executing contracts in a pharmaceutical or biotech company or Contract Research Organization (CRO). Clinical Trial Agreement (CTA) Management requires Knowledge of the pre-clinical clinical and periapproval drug development process required. Advanced skills in Microsoft Outlook Microsoft Word Microsoft Excel Microsoft Access Experience using Adobe Acrobat Professional and Microsoft Office SharePoint. Proficiency with specialized industry databases such as GrantPlan a plus. Must possess excellent skill ability in the following Project Management Clinical Trial Agreement (CTA) Management duties Develop CTA per patient budgets using Grant Manager. Draft study specific CTA templates. Finalize CTA templates and per patient budgets with study teams. Negotiate and establish pre-approval and approval workflows review roles task timelines and responsibilities and negotiation parameters with study teams. Draft negotiate and execute site specific CTAs within established study timelines and study budgets. Develop draft and negotiate CTA amendments within established study budgets. Assist with managing the Data Driven Payment process for assigned studies. Lead and coordinate CTA management for large studies. Lead and coordinate CTA management for all studies within a project. Draft negotiate and execute contracts and contract amendments for Pharmacology studies. Ensure contracts are executed within fair market standards as appropriate. Answer questions and resolve problems concerning all assigned studies and individual contracts. Track workflow and contract cost for all assigned studies and individual contracts.