SKILLS:

• Balance of general business, compliance, finance, legal, and drug development experience
• Precise communications and presentation skills
• Ability to plan, identify and mitigate risks to site contacting timelines
• Ability to lead by influence rather than positional power to accomplish critical deliverables
• Success in working in a highly matrix based organization
• Fluency in written and spoken English is required

KNOWLEDGE AND EXPERIENCE:

• 5+ years experience with clinical study budgets and clinical trial site contracting negotiation principles, practices, processes, and activities
• Knowledge of the principles, concepts and theories in applicable business discipline
• Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation preferred

EDUCATION:

• Bachelor’s Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR
• Juris Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing
  

  LI-CF1

JOB PURPOSE:

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.