Clinical Trial Registration Specialist
Princeton, New Jersey
Expiry Date :
Sun, 06 Dec 2020 23:59:59 GMT
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At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. One shared journey is moving us forward at Bristol Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. 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 the resources to pursue their goals, both at work and in their personal lives Responsibilities The Clinical Trial Registration Specialist will report to the Clinical Trial Registration Lead, prepare and provide operational support for the registration of clinical trials into public registries in US and EU. – Drives the processes for assigned protocol registration activity, resulting in timely, high-quality information posted on clinical trial registries ( and EU PAS) – Liaises with clinical team reviewers (Global Trial Managers, Operations Leads, Statisticians, Clinical Trial Physicians, Clinical Scientists, Development Leads, Patent Attorneys) and other stakeholders on all assigned trials to ensure trial registrations are accurate, consistent with the protocol and reported in adherence to NIH guidelines – Provides maintenance support to CT Registration Lead for assigned records, to ensure the accuracy of information disclosed on – Submits registration updates to on behalf of clinical team, within global regulatory timelines – Maintains study trackers and ensures they are up to date every week – Educates stakeholders, as needed, on NIH detailed review criteria for registrations as well as the purpose and format of patient-friendly fields in the protocol registration form Experience Requirements – Bachelor’s degree, preferably in Science – Minimum of 3 years overall work experience, preferably in a biopharmaceutical or CRO company – Demonstrated Excel and analytical skills – Ability to work in a global team and multiple therapeutic areas – Strong communication skills – Demonstrated ability to work independently and seek out support when needed – Written and oral communication skills – Strong organizational skills with the ability to multitask and prioritize – Work experience in quality, regulatory, compliance, clinical research or drug development highly desirable – Work experience in clinical trial transparency or clinical trial execution work, or work experience related to quality and compliance in clinical research preferred – US military experience will be considered towards industry experience requirements Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 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.