- Catalent Pharma Solutions (Greendale, IN)
- ** Site Deviation Investigator ** **Position Summary** + **Work Schedule:** Monday to Friday, business hours + 100% on- site in Greendale, IN Greendale is ... nutraceuticals via confection to enhance wellness for all consumers. The ** Site Deviation Investigator ** will be independently responsible for the efficient… more
- Lilly (Pleasant Prairie, WI)
- …of the quality of deviation investigations (post-approval). + Design and elaborate site deviation metrics. Participate in the review of plant deviation ... deviation assessment review pre-approval and post-approval. The Deviation mentor leads the site metrics related...and develop mitigation plans. + Trained as a lead investigator , deviation assessor and approver. Can act… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …crucial direction of the Head of Operations and the Head of Quality Systems, the Deviation Investigator will play a pivotal role in our company's growth by ... owning and investigating all Manufacturing-related deviations. The Deviation Investigator will collaborate with cross-functional stakeholders to perform simple… more
- Insight Global (Boston, MA)
- Job Description Insight Global is looking for a QC Analytical Investigator to sit on- site at a brand new facility in the beautiful Seaport district of Boston ... one of our top pharmaceutical clients. This is a first shift role, on- site Monday through Friday. This position will be supporting the growing technical services… more
- Bristol Myers Squibb (Bothell, WA)
- …records through the electronic quality record management system at BMS Bothell, WA. The Deviation Investigator on the MSAT team is an individual contributor role ... and determine the associated corrective action to prevent the deviation from reoccurring This person will be a key...experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location.… more
- University of Washington (Seattle, WA)
- …documentation for participation of all UW-affiliated medical institutions, such as investigator information, site certification, annual accrual figures, future ... Office (RSO) to meet all regulatory and compliance submissions involving editing of investigator initiated protocols and consent forms as well as submission of NCI… more
- University of Pennsylvania (Philadelphia, PA)
- …proposals, and research related presentations. Works closely with the Principal Investigator , manager, and study team to identify problems and develop solutions. ... needed and monitor results. Responsible for study coordination for investigator -initiated studies, multi-center research studies, and patient-oriented clinical and… more
- ThermoFisher Scientific (Suwanee, GA)
- …to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications + ... clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and… more
- University of Miami (Miami, FL)
- …standards and clinical credentials as delegated by the Principal Investigator . 6. Monitors, documents, reports, and follows-up on study unanticipated/adverse ... in implementing protocol amendments under direct supervision of the Principal Investigator . 8. Assists with study orientation and protocol related in-services to… more
- IQVIA (Troy, NY)
- …Description **Job Title:** Clinical Research Coordinator **Work Set-Up:** Working On- site **Schedule** : 16 hours per week. **Responsibilities:** + **Phlebotomy** ... signs.** + Coordinate clinical research studies conducted by a supervising principal investigator . + Update and maintain skills, training, and knowledge of current… more