Job Description
As a Site Contract Management Associate - you will be joining the worldβs largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations. Responsible for delivery on established targets/measurements. Work with global teams to review and analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions.
Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Analyze investigator fees in relation to fair market value pricing and ensure alignment with regional standards and the J&J pricing guidelines. Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required. Manage the contract amendment lifecycle. Assume responsibility for all aspects of legal document and metrics tracking. Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.
About ICON
ICON is the worldβs largest & most comprehensive clinical research organisation, powered by healthcare intelligence.