- Parexel (Jefferson City, MO)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards. The Sr....sites and will work closely with the Site Care Partner (SCP), and other members of the study team,… more
- Parexel (Jefferson City, MO)
- The Site Care Partner is a crucial liaison for investigative sites throughout a study's lifecycle, responsible for site start-up, activation, relationship ... ensure site readiness for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of… more
- Parexel (Jefferson City, MO)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr. CRA...sites and will work closely with the Site Care Partner (SCP), and other members of the study team,… more
- Parexel (Jefferson City, MO)
- …innovative clinical research and regulatory solutions. As a leading global clinical research organization (CRO), we partner with the world's most prominent ... audit requirements in a GxP environment. + Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations,… more
- Parexel (Jefferson City, MO)
- …and/or operational performance data and presenting as an integral member of the Clinical Study team for clinical development studies. The reviews include ... requiring intervention. + Facilitate Study Team Decisions: Present findings to clinical study teams, support root cause analysis, and provide recommendations for… more
- Parexel (Jefferson City, MO)
- …facilitate timely endorsement of labeling decisions by senior leadership. + Interpret clinical and scientific data to inform labeling content and product claims; ... regional implementation of CDS updates and monitor compliance across markets. + Partner with regional and local regulatory leads to address Health Authority… more
- Cordis (Springfield, MO)
- …existing accounts + Demonstrate outstanding product knowledge, understanding of related clinical data, competitive product knowledge, & overall industry trends + ... be able to support their needs in the lab + Effectively partner with Cordis leadership, cross-functional teams, & field-based counterparts (Regional Directors,… more
- Endo International (St. Louis, MO)
- …quality control teams, oversees daily quality operations, and serves as a key partner to site leadership by providing guidance on quality and compliance across the ... customer focus. _Skills/Competencies:_ + Strong writing skills to effectively communicate technical/ clinical information to others. + Ability to use various software… more
- SSM Health (Jefferson City, MO)
- …SSM Health upon hire or if hired in Oklahoma/Wisconsin, completion of the Clinical Partner I orientation checklist during 90 day orientation/probationary period. ... EXPERIENCE + No experience required. PHYSICAL REQUIREMENTS + Constant standing and walking. + Frequent use of hearing and speech to share information through oral communication. + Frequent use of hearing to distinguish body sounds and/or hear alarms,… more
- SSM Health (Jefferson City, MO)
- …SSM Health upon hire or if hired in Oklahoma/Wisconsin, completion of the Clinical Partner I orientation checklist during 90 day orientation/probationary period. ... EXPERIENCE + No experience required PHYSICAL REQUIREMENTS + Constant standing and walking. + Frequent use of hearing and speech to share information through oral communication. + Frequent use of hearing to distinguish body sounds and/or hear alarms,… more
