• Engaging with Healthcare stakeholders on legal and budget negotiations. • Managing software tools such as ICD, and Veeva Vault specifically used to review, and approve, in-house Agreements • Involved in the protocol projects from the start - end process for company-sponsored and/or investigator-initiated studies. • Partnering with Healthcare Compliance, Risk Management, Privacy, Legal, and other stakeholders on optimization of the IT procedures regarding contracting. • Monitor non-productive or non-responsive third parties throughout the negotiation a establish a follow-up plan. • Providing recommendations to improve processes and establishing refinements that reduce cycle time, create savings, and improve efficiency in the initiation of clinical trial sites., Pharmaceutical Procurement, Biopharmaceuticals, gsk, Biopharmaceuticals, European commission, EU, Pharmacovigilance, Pharmaceutical