Bristol Myers Squibb Work Values

Daily Duties at Bristol Myers Squibb:

Lead Site Manager/Project Management, Early Phase Monitoring to Establish Potential Efficacy, Phase 2, Phase 3, Site Selections, Collaboration, Study Start Up, Selection of CRO/Selection of all Vendors and Contracting (if not in-house managed), Safety monitoring, AE assessment, SAE reporting, submissions to FDA. Oversight of Sites and Vendors, Monitoring Site Visits, Co-monitoring, Site Staff Training and Engagement Activities (on site training, Skype training or investigator meeting), Compliance oversight, including appropriate subject enrollment, SAE filing and follow-up, medical writing for FDA submissions at required intervals/immediate submission.

What they like about Bristol Myers Squibb:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

Clinical Research, Oncology, Immunology, Neuroscience, CRA, Registered Nurse, Clinical Manager, Data Management, Clinical Oversight, Project Management, CRO, CRO Oversight, GCP, ICH, Pharmaceutical Industry, Clinical Site Management, Compliance, Safety Management, Site Selection, Regulatory Compliance, Continuous Quality Improvement, Medical Writing, FDA Reporting, Trial Master File/eTMF, Cross-Functional Facilitation, Strategic Planning, Risk Analysis, Safety Oversight and Reporting, Data Targeted Review

Skills

Team Leadership, Clear, Concise Communication, Think "outside the box", Creativity, Problem Resolution, Evaluation With Recommendation, Teamwork, Provide Feedback, Listening Skills

These are some of the questions we asked our climbers about their experiences with Bristol Myers Squibb: