Are you a Regulatory Affairs professional looking to work independently and take ownership of the writing of CMC sections of DMF, BLA, and NDA submissions? Have you supported full product development activities from pre-clinical/clinical to FDA submissions? Are you interested in helping a company expand their client base in new countries? Do you have experience independently writing CMC sections of global regulatory submissions? This position could be for you!
If you're interested in a Lead Regulatory Affairs Specialist position with a well established pharmaceutical company in Madison, Wisconsin, apply here for more details!
...Job Title: Field Outreach Specialist Location: Scottsdale, AZ Duration: 3-6 Months Work Type: Part-Time - (Flexible Work Hours) Key Responsibilities: Research and identify local tech organizations for partnership opportunities. Assist in planning and...
Pride Health is hiring a Special Investigative Unit Investigator for one of its clients in Michigan. This is a 12-week contract with a possible extension, with competitive pay and benefits. This position is remote, but candidates MUST be in Eastern or Central ...
...Education assistance through MyQuest for Education ~ Career advancement opportunities and so much more! Science Director, Immunology Onsite in San Juan Capistrano, CA Quest Diagnostics is a leading provider of clinical laboratory testing for the diagnosis and...
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...Job Duties: Under supervision the RN performs all duties of comprehensive behavioral health nursing services as qualified to provide to include but are not limited to: RNs work experience with either Mental Health, Acute Care and Co-occurring Mental health settings...