Regulatory CMC Expert

5 days ago


South San Francisco, California, United States ORIC Pharmaceuticals Full time
Job Description

We are seeking a highly skilled Regulatory CMC Expert to join our team at ORIC Pharmaceuticals. As a key member of our Pharmaceutical Development group, you will play a critical role in supporting the development of novel therapeutics for treatment-resistant cancers.

Responsibilities:
  • Support the internal PharmDev teams in advancing the nonclinical and clinical development of small molecule therapeutics.
  • Collaborate closely with cross-functional teams, including Regulatory Affairs, Quality Assurance, Finance, Commercial, and Supply Chain.
  • Maintain and update a CMC risk register, track action items against identified risks, and communicate status periodically.
Qualifications

Applicants should have a BS or MS or PhD in a relevant pharmaceutical sciences discipline and 2-6 years of experience in drug discovery and development. Strong project management skills, including budgeting, planning, and visualization tools, are essential. Familiarity with ICH, GMP, quality systems, and regulatory guidances is also required.

The estimated annual salary for this position is $127,500, based on national averages and industry standards.



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