Site Contract Specialist

Prepare, review, negotiate, and finalize clinical site contracts and investigator budgets using approved templates and standards Partner with internal teams and external research sites to support timely contract execution aligned with study timelines Ensure accuracy, completeness, and quality of contract documentation in approved systems Identify and proactively address routine contracting questions while escalating non‑standard items as appropriate Support operational metrics related to quality, cycle time, and data accuracy Contribute to process improvements by identifying trends, recurring issues, and opportunities to enhance efficiency Maintain strong collaboration with legal, finance, clinical operations, and external partners. Supporting People with Disabilities Bachelor's degree in Life Sciences, Business Administration, or a related field Experience in clinical trial contracting, clinical operations, or a related pharmaceutical or research environment Strong attention to detail and ability to manage multiple priorities simultaneously Effective written and verbal communication skills in a global, multicultural environment Ability to work collaboratively and apply structured processes in a regulated setting Proficiency with contract management systems and standard business software tools Experience supporting clinical studies Familiarity with investigator grants and site budget negotiations Experience working with electronic contract or document management systems