Protocol Model Document Content Steward
Warsaw, PolandPosted Jun 19, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsProtocol Model Document Content StewardWarsaw - PLApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.What if your work shaped the blueprint for life-changing clinical trials?Every groundbreaking medicine that reaches a patient starts with a protocol. And every protocol starts with a document that has to be precise, compliant, and built to last. That's where you come in.At BMS, we're looking for a Protocol Model Document Content Steward - someone who takes genuine pride in the craft of clinical documentation, who sees structure and governance not as red tape, but as the foundation that keeps patients safe and science moving forward.This isn't a back-office role. This is a position at the heart of drug development, where your fingerprints are on every clinical trial we run.So, what will you actually be doing?Think of yourself as the guardian of clarity and consistency across BMS's global clinical trial portfolio. You'll own the Model Documents that underpin Study Protocols - ensuring they're always current, always compliant, and always ready for whatever regulators, investigators or health authorities need to see.Here's what that looks like day-to-day:You'll be the expert in the room. When colleagues across Drug Development, Regulatory, Legal, Safety, Medical Affairs and beyond need guidance on clinical trial documentation standards, they'll turn to you. You'll develop a deep mastery of ICH guidelines, GCP requirements and industry standards and translate that expertise into documents people can actually use.You'll collaborate across the whole enterprise. This role connects you with virtually every function in R&D. From IT to Translational Medicine, from outsourcing teams to CROs and external partners - you'll build relationships and influence decisions across geographies and disciplines. If you thrive on variety and cross-functional energy, you'll love this.You'll represent BMS externally. You'll engage with industry bodies like TransCelerate, PhRMA and EFPIA, helping shape industry-wide standards - not just follow them. You'll align BMS's Model Documents with the TransCelerate Protocol Model Document, putting you at the forefront of industry collaboration.You'll be inspection-ready,...