Site Contract Specialist

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Summary The Site Contract Specialist plays a critical role in enabling clinical trials by supporting the preparation, negotiation, and finalization of site contracts and investigator budgets. This role contributes directly to timely study start‑up and execution by working closely with cross‑functional partners and external research sites. You will be part of a team focused on operational excellence, quality, and collaboration, supporting studies across multiple regions while contributing to continuous improvement and standardization efforts within clinical trial operations.

This position is responsible for managing site contracting activities within established frameworks and processes, ensuring accuracy, consistency, and compliance. The role offers the opportunity to develop strong negotiation skills, build cross‑functional partnerships, and gain exposure to clinical research operations. This is an ideal opportunity for someone motivated by structured problem‑solving, collaboration, organization, and making a tangible impact on clinical trial delivery.

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.

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 Strong MS office skills Preferred Qualification Experience supporting clinical studies Familiarity with investigator grants and site budget negotiations Experience working with electronic contract or document management systems We are seeking to fill multiple Site Contract Specialist roles as part of our new build! #LI-Hybrid We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Overview: Warsaw - PL: zł180,200 - zł218,360
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated