Regulatory and Site Start Up Specialist
Precision for Medicine(13 days ago)
About this role
A Regulatory and Site Start Up Specialist at Precision for Medicine supports regulatory and site start-up functions for clinical trials, with a focus on oncology and rare disease. Based in Shanghai or Beijing, the role operates within the company's integrated clinical, laboratory, and data sciences environment to help enable timely and compliant trial execution.
Required Skills
- Regulatory Submissions
- Site Start-up
- ICF Review
- Essential Documents
- Project Planning
- Stakeholder Communication
- Contract Negotiation
- Milestone Tracking
- Translation Coordination
- TMF Maintenance
+1 more
Qualifications
- Bachelor's Degree Life Sciences
- Registered Nurse
- MD
- PhD
- PharmD
- RAC Certification
- Master's Regulatory Science
About Precision for Medicine
precisiongroupcompanies.comThe site is currently a placeholder that immediately redirects to /lander and contains no public content describing the company. Presuming it's a web-focused startup, it likely offers a SaaS platform to help businesses build high-converting landing pages and marketing funnels. Typical offerings would include a drag-and-drop page builder, A/B testing, analytics, and integrations with CRMs and email platforms to drive lead generation. Customers would be small-to-medium businesses and marketing teams seeking easy onboarding, template libraries, and conversion optimization tools.
Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Precision for Medicine
Similar Jobs
Clinical Trial Specialist
Aegis Ventures(14 days ago)
Sr. Clinical Trial Manager Consultant
ClinChoice(5 days ago)
Clinical Trial Manager Consultant - II
ClinChoice(7 days ago)
Clinical Trial Manager Consultant - II
ClinChoice(5 days ago)
Sr. Manager, Study Start-Up
Alimentiv(29 days ago)
Associate Director, Clinical Scientist
Umoja Biopharma(26 days ago)