Clinical Trial Associate Jobs in Omaha, NE

Medical Director (DVM) Omaha NEA progressive small animal practice in Omaha Nebraska is seeking a compassionate and experienced Medical Director to lead its veterinary team and drive clinical excellence. This is an ideal opportunity for a skilled veterinarian ready to take the next step into a lead...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Medical Director (DVM) Omaha NEA progressive small animal practice in Omaha Nebraska is seeking a compassionate and experienced Medical Director to lead its veterinary team and drive clinical excellence. This is an ideal opportunity for a skilled veterinarian ready to take the next step into a lead...

Why work for Nebraska Methodist Health SystemAt Nebraska Methodist Health System we focus on providing exceptional care to the communities we serve and people we employ. We call it The Meaning of Care a culture that has and will continue to set us apart. Its helping families grow by making each del...

OverviewClinical Liaison ( RN / RRT )Select Specialty HospitalCritical Illness Recovery Hospital (LTACH)A day in the lifeYoull advocate for referred patients in the pre-admission process by collaborating with clinical teams to assess patient needs. You will serve as a resource for healthcare profess...

Responsibilities: The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global regulatory require...

Responsibilities: The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS) Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products including regulatory responsibilities in associated change control and labeling proc...

Responsibilities: The Senior Manager Regulatory CMC Technical Writing and Submission Management role will be responsible for supporting the authoring compiling and management of CMC sections for global regulatory filings. This role requires a strong understanding of the drug development process pha...