Site Contracts Manager Jobs

Significant experience negotiating legal language and budgets as it relates to clinical trial study agreements.

Experience in Pharmaceuticals or Biotechnology, and experience managing and/or working with CROs.

Demonstrated leadership skills, networking skills, and communication skills.

Determining an acceptable range of fees and conditions specific to each trial and country and clinical site.

Collaborating with the CPM regarding support from Legal, IP Legal, Compliance and other relevant stakeholder groups, where needed.

Providing instructions and support to the CRO during the negotiation with the clinical sites/investigators.