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Nonclinical Scientist, Regulatory Affairs & Product Development

Overland, KS 66210

Posted: 09/17/2024 Employment Type: Contract Job Category: Regulatory Sciences and Medical Writing Job Number: 614072 Is job remote?: Yes Country: United States

Job Description

Target PR Range: 100-120/hr
  Duties:
Job Title: Nonclinical Scientist, Regulatory Affairs & Product Dev
Regulatory Affairs

 

Regulatory Affairs & Product Development is responsible for nonclinical development consulting to provide innovative solutions and regulatory submissions for all aspects of pharmaceutical, biologics and device development from discovery through post-approval maintenance.


Job Duties:
  • Utilizes broad and deep knowledge to develop innovative new business practices, policies, and procedures.
  • Contributes to the development of department strategy.
  • Works on or may lead highly complex projects of large scope.
  • Projects are typically cross-functional and have significant and long-term impact.
  • Provides solutions which set precedent.
  • Negotiates complex or risky technical business issues on behalf of the company.
  • Independently defines project establishes budgets identifies participants and mitigates risk.
  • Consults with management to determine project objectives with long-term implications.
  • Acts as a mentor to less experienced colleagues
Skills:
•    12+ years of experience, preferred
•    Ability to work independently
•    Strong knowledge of regulations/guidelines required

•    Scientific and technical reading, writing and editing skills required.
•    Well-developed organizational, interpersonal and communication skills, and the ability to develop and present varied and unique ideas.
 • Good working knowledge of MS WORD, Adobe Acrobat, Project, Powerpoint and use of one or more electronic document management systems
Education:
Bachelor's degree in related field, or equivalent work experience
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About Overland, KS

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