- ThermoFisher Scientific (Worcester, MA)
- …people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world ... Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards , Laboratory Setting **Job Description** **Associate Scientist - FSP -… more
- Houston Methodist (Houston, TX)
- …information, facilitating and directing implementation of evidence-based practice using data and performance improvement methodologies. This position must be ... overseeing and designing the review, analysis, and integration of data in the workflow design to support organization and...all levels of the organization, from front-line clerical and clinical personnel to senior management and medical staff and… more
- Bristol Myers Squibb (Summit, NJ)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... knowledge of ISPE guidance, 21 CFR Part 1, and Data Integrity compliance. + Strong working knowledge of SDLC...compliance. + Strong working knowledge of SDLC principles and standards . + Ability to work with the end user… more
- Globus Medical, Inc. (Audubon, PA)
- …of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and ... will play a critical role in driving the commercial success of our global medical device business. This individual will partner closely with regional sales leaders… more
- Catalent Pharma Solutions (San Diego, CA)
- …8am-5pm + 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent's San Diego facility ... preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego… more
- Bristol Myers Squibb (Tampa, FL)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... goals and employee needs. The Senior consultant will be responsible for data management, and enhancement of benefits offerings, working closely with the benefits… more
- Bristol Myers Squibb (Tampa, FL)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... integrations (files) between HR system, payroll system, benefits systems, ensuring data files are accurate. + Operationalizes the annual BEP/savings elections,… more
- Bristol Myers Squibb (Indianapolis, IN)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... actions as required. + Develop and maintain appropriate documentation, particularly data analysis. + Ensure compliance with GMP regulations, safety guidelines, and… more
- Parexel (Baton Rouge, LA)
- …proposals, budgets, timelines, and milestones** while ensuring compliance with SOPs and data privacy standards . + Collaborate with multidisciplinary teams to ... and deliver innovative Real World Research (RWR) solutions for global clients. This is a great opportunity to join...adaptability, and a go-getter mindset. Experience in **RWD/RWE** , ** data privacy** , and **drug development** is a plus.… more
- Medtronic (Houston, TX)
- …policies and procedures + Adheres to financial, regulatory, quality compliance standards and requirements. **Influence and Selling:** + Identify, establish and ... expectations and improves outcomes when supporting cases. + Engages physicians in clinical conversations about advantages of the therapy and products. + Conducts all… more