*This role is to consider experienced candidates (minimum 2 years) with AUS/ NZ site contracting/ budget negotiation from either CRO or Pharmaceutical company setting/ working environment.*
Investigator Contracts Lead I (ICL I) is responsible for direct site facing contract and budget negotiations through contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (pCRO) and collaborating with other lines to plan site contracting timelines though start up.
Key Accountabilities:
Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters
Interacts with clinical site contracts & legal contacts, client and partner legal team, study management, site payments team, peer site contracting colleagues, CRO site contracting teams
Compliance with Parexel standards
Balance of general business, compliance, finance, legal, and drug development experience
Knowledge and Experience:
Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities
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