EPM Scientific
This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $250,000.00/yr - $350,000.00/yr
Director, Clinical Development [Medical Director]
Job Type: Full-time
Location: Remote [must be based in California]
Company Summary: A clinical stage biotech harnessing best-in-class siRNA therapeutics is growing their US clinical team as they have 3 clinical stage assets in studies across US, AUS, and China.
Key Responsibilities
Reports directly to CMO (based in CA)
Design/execute global CDPs (including China), draft protocols/IBs, and ensure FDA/EMA/NMPA alignment.
Oversee trial execution (US/China/Australia), ensuring ICH/GCP compliance, data integrity, and risk mitigation with CROs/sites.
Collaborate cross functionally (regulatory, CMC, BD) and externally (CROs, investigators) to prioritize resources and harmonize global strategies.
Drive audit ready compliance, lead clinical training for internal/external teams, and optimize operational processes.
The Opportunity: Join a leader in the nucleic acid therapy space as an experienced individual contributor with the opportunity to design & execute clinical development plans on a global scale.
Qualifications
MD (7+ years clinical training)
5+ years senior clinical development leadership (in biotech OR pharma)
Cardiovascular/internal medicine expertise preferred; RNA/cell/gene therapy experience a plus.
Proven success navigating China (NMPA), US (FDA), and Australia regulatory pathways.
Fluent English & Chinese (oral/written); proven ability to lead matrixed teams across US-China-Australia.
If you're interested, please drop a CV and we'll be in touch if it's a good fit.
#J-18808-Ljbffr
Base pay range $250,000.00/yr - $350,000.00/yr
Director, Clinical Development [Medical Director]
Job Type: Full-time
Location: Remote [must be based in California]
Company Summary: A clinical stage biotech harnessing best-in-class siRNA therapeutics is growing their US clinical team as they have 3 clinical stage assets in studies across US, AUS, and China.
Key Responsibilities
Reports directly to CMO (based in CA)
Design/execute global CDPs (including China), draft protocols/IBs, and ensure FDA/EMA/NMPA alignment.
Oversee trial execution (US/China/Australia), ensuring ICH/GCP compliance, data integrity, and risk mitigation with CROs/sites.
Collaborate cross functionally (regulatory, CMC, BD) and externally (CROs, investigators) to prioritize resources and harmonize global strategies.
Drive audit ready compliance, lead clinical training for internal/external teams, and optimize operational processes.
The Opportunity: Join a leader in the nucleic acid therapy space as an experienced individual contributor with the opportunity to design & execute clinical development plans on a global scale.
Qualifications
MD (7+ years clinical training)
5+ years senior clinical development leadership (in biotech OR pharma)
Cardiovascular/internal medicine expertise preferred; RNA/cell/gene therapy experience a plus.
Proven success navigating China (NMPA), US (FDA), and Australia regulatory pathways.
Fluent English & Chinese (oral/written); proven ability to lead matrixed teams across US-China-Australia.
If you're interested, please drop a CV and we'll be in touch if it's a good fit.
#J-18808-Ljbffr