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: Workday Project Manager Location: Hybrid from Richmond, VA (3 days per week from Office) Job Type: Contract Job Description... ...of Workday implementation, enhancement, or AMS projects across HCM and Finance modules. This role requires strong program...
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...be part of a growing business while making a difference in the lives of children. Prior experience in a childcare setting a plus on weekdays but a MUST for weekend admin. The program values great leadership and opportunity for growthDay to day operations Operations....
POSITION: COACH & VOLUNTEERSWe are in need of Rock Steady Coaches. We also need Volunteers to assist the Coaches. A Coach should have... ...s disease to fight their disease by providing non-contact boxing style fitness programs that improve their quality of life and...