- Baylor Scott & White Health (Dallas, TX)
- …adjusts therapies as indicated. + For credentialed professionals, acts as a clinical specialist in diabetes insulin management. Supports transplant patients with ... **Transplant Nutrition Specialist ** **Full Time Day Shift** **: 8AM-5PM** **Location: 3410 Worth St Dallas, TX** **CDCES certification required** **About Us** Here… more
- Sharp HealthCare (Santee, CA)
- …medical necessity reviews) based on department and regulatory requirements.PT Spec II additional standardsSupports clinic needs for documentation review and ... and providers. Serves as a mentor across all PT clinics. Develops and implements clinical programs in support of all PT clinics' pursuit to provide the Sharp… more
- Fujifilm (College Station, TX)
- …of the Data Integrity projects at FUJIFILM Biotechnologies, Texas. The Quality Assurance (QA) Specialist II for Data Integrity will be responsible for the day to ... Quality management to implement quality systems that will enable cGMP manufacturing of pre- clinical to commercial products. + Work as a change agent to compliantly… more
- Abbott (Plymouth, MN)
- …160 countries. Job Description WHAT YOU'LL DO We are recruiting for a Regulatory Operations Specialist II , to join our team in the Plymouth, MN location. In this ... and modified products globally. * Acts as a regulatory representative responsible for review and analysis of GTS blocked orders, providing guidance and direction on… more
- UTMB Health (Galveston, TX)
- Research Development Specialist II (Hybrid) Vice President For Research **Galveston, Texas, United States** Research Academic & Clinical UTMB Health ... of hypotheses, aims, and objectives, grantsmanship and limited scientific review . + Proposal development duties include obtaining competitive intelligence on… more
- BD (Becton, Dickinson and Company) (Louisville, CO)
- **Job Description Summary** The Regulatory Affairs Specialist II is responsible for implementation of strategies including domestic and international submissions ... with FDA and international reviewers and respond to questions + Provide timely review and approval of product labeling and marketing claims for regulatory compliance… more
- AnMed Health (Anderson, SC)
- …all required patient types within defined review standards, including daily review for discharges and transfers. + Uses clinical knowledge to independently ... include but are not limited to initial medical necessity review , continued stay/concurrent review , retrospective review... review the medical record for clinical appropriateness and resource utilization including but not limited… more
- Bristol Myers Squibb (Summit, NJ)
- …The MS&T Manufacturing Systems Engineering and Operations - Manufacturing Systems Engineer II is responsible for supporting the solution intake and design, delivery, ... in the production of personalized cell therapy products for both global clinical trials and commercial supply. The incumbent must be self-directed, goal-oriented,… more
- Kelly Services (Winston Salem, NC)
- **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem NC** **Contract Role, 12 month long with potential to convert** **Hourly Pay Rates: ... product freezing and storage, and driving continuous improvement. The Manufacturing Specialist III is also responsible for mentoring team members, leading… more
- Guthrie (Sayre, PA)
- Position Summary: Fulfills all requirements of Insurance Specialist I, as well as serving as a group leader by participating in staffing and employment issues. ... Serves as a resource specialist within the department. Trains Insurance Billing Specialists I...worked in combination with Management, Compliance, Medical Records and Clinical Operations. 9. Serves as a group leader by… more