PFor one of our clients, a global health care company, we are looking for an experienced Clinical Contracts Specialist.br / br / strongJob Description /strongbr / As Clinical Contracts Specialist, you are responsible and accountable for activities related to the preparation, negotiation and signature of clinical trial contracts and budgets.br / br / strongResponsibilities /strong /pulliYou are responsible for drafting, reviewing, and editing contracts, master agreements, amendments, and related documents. /liliYou collaborate with Legal and other key stakeholders to address contract language concerning specific topics to ensure compliance. /liliIn alignment with company policies, applicable regulations, and guidance from the Legal Department, you negotiate contract terms with research sites. /liliYou serve as the primary point of contact between the site and the project team for all contractual matters, resolving issues and clearly communicating the agreed approach. /liliYou lead negotiations with research sites to ensure that clinical trial site budgets align with protocol requirements and company policies. /liliYou obtain necessary management approvals for budget items that exceed departmental compliance thresholds, supported by appropriate justification documentation. /liliYou maintain close communication with the Legal Team to ensure adherence to legal requirements and client policies. /liliYou advise your manager on potential challenges and work collaboratively to meet contractual obligations and timelines, ensuring milestones and commitments are communicated and achieved. /liliYou maintain communication of negotiation status using Company IT systems. /liliYou meet study site activation timelines utilizing effective negotiations skills which results in signed executable agreements. /liliYou participate in site activation calls. /liliAs required, you coordinate and/or support Clinical HCP Agreements in the assigned region.br / /li /ulpstrongRequirements /strong /pulliBachelor's degree or master's degree in Life Sciences or any other orientation with a first experience in clinical trials. /liliExperience in clinical research as well as in contracting ideally. /liliFluent in English, any other language is an asset. /liliProactivity and adaptability are key. /liliGood communication skills. /li /ulpbr / strongContract information /strong /pulliPermanent contract with Oxford Global Resources. /liliOffice-based position in a dynamic, international environment. /liliFull time required. /liliStart date in January 2026. /li /ul