- ICON Clinical Research (Brentwood, TN)
- …to the Central CDP Review Team (CDPRT) and Sponsor. **What you need for Study Start Up Associate I - Regulatory Submissions** * A high school diploma or ... Study Start Up Associate ... Study Start Up Associate II - US,...regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor… more
- Colorado State University (Fort Collins, CO)
- … studies are conducted according to protocol and meet regulatory requirements. Percentage Of Time20 Job Duty CategoryStudy Conduct Procedures Duty/Responsibility ... Posting Detail Information Working TitleRA II - Study Lead, ARPA H Position LocationFort Collins, CO...studies are conducted according to protocol and meet regulatory requirements Percentage Of Time10 Application Details Special Instructions… more
- Dana-Farber Cancer Institute (Boston, MA)
- …reporting for the DFCI. The CRM will be supervised and supported by the Associate Director of Cohort Studies to develop and implement strategies that will ... Studies program. + Initiates, plans, facilitates and oversees the research project start -up, active and close out phases; for studies and activities within… more
- Actalent (Basking Ridge, NJ)
- …for Operational Study Strategy. Responsibilities + Develop project cross-functional, integrated study plans to study start -up (in-house) and validate and ... Study team. This role is primarily a tactical study delivery role, reporting into an Associate ...documents are created in a timely manner ahead of study start . + Coordinate with the CRO… more
- Battelle Memorial Institute (Columbus, OH)
- …quality control (QC) in electronic data acquisition systems + Assist with study start preparation activities including requests for equipment, ordering ... critical services for our clients-whether they are a multi-national corporation, a small start -up or a government agency. We recognize and appreciate the value and… more
- Cargill (Wichita, KS)
- …around the world and connect with something greater. **Food Safety, Quality, and Regulatory Associate Position:** The purpose of this position is to develop ... if your ideas could nourish the world? As an associate , we transfer your knowledge and skills into profound...of increased complexity across the Food Safety, Quality, and Regulatory (FSQR) job family at various locations across Cargill.… more
- AdventHealth (Orlando, FL)
- …maintenance for AdventHealth Research Institute (AHRI) research activities. The Research Regulatory Specialist I, coordinates the research protocol start -up ... study team are reviewed and approved._ _Ensure all regulatory documents, including all Essential Documents as defined by...and administration in a courteous and professional manner._ _Ensures regulatory documents for all closed studies are… more
- University of Utah (Salt Lake City, UT)
- …submission and management; industry sponsored study start -up and close out. **Responsibilities** ** Regulatory /Compliance/General Responsibilities** ... Details **Open Date** 11/12/2024 **Requisition Number** PRN40316B **Job Title** PS Regulatory Coordinator **Working Title** PS Regulatory Coordinator **Job… more
- Penn Medicine (Plainsboro, NJ)
- …regarding process. Ensure process moves steadily to completion, clear roadblocks to study start up.COMPLIANCE: Perform group-specific regulatory activities, ... research portfolio. This employee will oversee the processes for study start -up and on-going study ...start to finish working closely with the CRU Regulatory coordinators to manage, review, and initiate trials to… more
- Abbott (Alameda, CA)
- …generating monitoring trip reports, and track resolution of action items. + Participate in study start up activities. + Responsible for ensuring shipment of ... but not limited to planning and implementation of clinical studies from concept to clinical study report...+ Participate in the interim and final reviews of study data in preparation of regulatory submissions.… more