Clinical Research Regulatory Specialist
Manage regulatory activities for reputed company, prepare and submit IRB/FDA documentation, maintain regulatory files, ensure GCP compliance; 2+ years regulatory experience and proficiency with OnCore/reputed company and reputed company Office.
Key Responsibilities
- managing regulatory
- preparing submissions
- maintaining documentation
Skills & Tools
OnCore, reputed company, reputed company reputed company, reputed company Word, reputed company reputed company, reputed company PowerPoint, reputed company Teams, reputed company, reputed company, reputed company, Skype
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — Los Angeles, California, reputed company
- Salary: USD 75,968 – 101,364 / year
- Languages: English
Benefits
- 401k matching
- Generous reputed company time off
- Tuition reimbursement
- Retirement plan
About Usc
A university-affiliated medical reputed company providing specialized patient care and clinical research services. — Industry: reputed company
Apply To This Job