- Bristol Myers Squibb (Indianapolis, IN)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... to be the global leader in radiopharmaceuticals. **Summary** The Document Control Specialist is responsible for the tactical oversight and maintenance of document… more
- Merck (Omaha, NE)
- …+ Awareness of diversity. \#MSJR **Required Skills:** Adaptability, Adaptability, Audit Management, Clinical Trials , Clinical Trials Operations, ... **Job Description** This position within our company's Global Clinical Supply Compliance Operations responsible for ensuring imports/exports are declared and shipped… more
- Banner Health (Gilbert, AZ)
- …has served over 1.5 million patient visits and is home to nearly 200 active clinical trials . Prior RN Experience Required in this role **Schedule** : Exempt, ... with multidisciplinary teams. 2. Develops and analyzes data for administrative and clinical decision making, as well as regulatory requirements. Coordinates… more
- Bristol Myers Squibb (Bothell, WA)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... more: careers.bms.com/working-with-us . The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for BMS Jump… more
- Parexel (Helena, MT)
- …or related industry experience + Extensive previous experience of working in a Start-up team, Clinical Trial Specialist , CRA, Clinical Trial Manager ... activities in the matrix, by working closely with the Clinical Trial Manager and CRO counterparts. +...processes, and ensure timely execution of clinical trials that align with project objectives and regulatory… more
- Bristol Myers Squibb (Summit, NJ)
- …used in the production of personalized cell therapy products for both global clinical trials and commercial supply. The incumbent must be self-directed, ... and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
- Bristol Myers Squibb (Devens, MA)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... In the capacity of Shop Floor QA, the Senior Specialist shall serve as one of the Shop Floor...research, understand, interpret and apply internal SOP's, policies and regulatory guidelines. + Proficient computer skills with knowledge of… more
- University of Miami (Miami, FL)
- …+ Visits appropriate referral sources (ie hospitals, clinics, etc.) to market clinical studies/ trials and conducts face-to-face screenings and assessments to ... has an exciting opportunity for a full-time Research Support Specialist to work onsite on the UHealth campus. The...Assists with the preparation of grant proposals by processing regulatory documents for all institutions and offices involved. +… more
- Cedars-Sinai (Beverly Hills, CA)
- …/IRB operations from start-up to closeout. + Serves as sub/co-investigator on clinical trials , observational research, and biobanking protocols. + Responsible ... partners. Implements recruitment strategies and workflows to ensure top enrollment in global clinical trials . + Obtains informed consent for clinical … more
- University of Pennsylvania (Philadelphia, PA)
- …with collaborating sites and external institutions, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry ... to provide assistance and oversight with single-center and multi-center clinical research trials conducted within the Cardiovascular... regulatory files per GCP. + Work with Regulatory Affairs Specialist to prepare for audits,… more