- Sumitomo Pharma (Annapolis, MD)
- …lead the design of clinical studies in close collaboration with the Clinical Research Team. + Monitor protocol compliance including assessment of inclusion ... motivated, and experienced individual for the position of **Senior Clinical Research Scientist.** This is an exciting opportunity to...+ Comprehensive understanding of the drug development process from Phase 1 to Phase 3. + Prior… more
- University of Maryland, Baltimore (Baltimore, MD)
- …Medicine to lead and ensure the excellence of the educational, scientific, and clinical programs within the School of Medicine, Medical Center, and Medical System. ... for operations and strategy of the Department of Medicine's clinical , research, and educational programs, including internal medicine subspecialties. The… more
- Johns Hopkins University (Baltimore, MD)
- …disease for other healthcare professionals. + Coordinate and act as a sub-investigator in phase II, III, and IV clinical trials. This includes preparing and ... patients sign pain contracts, refilling medications, and tracking prescribed narcotics. + Monitor patients while on therapy to evaluate for side effects and to… more
- Catalent Pharma Solutions (Harmans, MD)
- …CGMP manufacturing suites and cold storage warehousing._ _Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including ... observing manufacturing operations and reviewing documentation for compliance. Continuously monitor systems and procedures to ensure compliance with applicable… more
- Catalent Pharma Solutions (Harmans, MD)
- …CGMP manufacturing suites and cold storage warehousing. Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including ... observing manufacturing operations and reviewing documentation for compliance. Continuously monitor systems and procedures to ensure compliance with applicable… more
- Amergis (Madison, MD)
- …reduce recidivism in the juvenile justice system. Treatment approach involves a multi- phase therapeutic process that works first to establish a foundation of trust, ... medical files and documentation + Ensure adherence to HIPAA standards. + Monitor and maintain compliance with all applicable healthcare regulations. + Oversee… more
- Charles River Laboratories (Rockville, MD)
- …for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Key Responsibilities and Duties: Establishes… more
- Charles River Laboratories (Rockville, MD)
- …for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. This includes but is not limited to the… more
- Charles River Laboratories (Rockville, MD)
- …for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. **Key Responsibilities and Duties:** *… more
- Catalent Pharma Solutions (Harmans, MD)
- …CGMP manufacturing suites and cold storage warehousing._ _Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including ... to clients and on cross-functional project teams. + Execute and monitor critical processes supporting mammalian and microbial production facilities- extensive… more