Strategic Leader, Global Clinical Development

Immix Biopharma (Nasdaq: IMMX); Los Angeles (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

Immix Biopharma is seeking an Associate Director, Clinical Development in Los Angeles to lead protocol drafting for new indications and interpret complex trial data. You will coordinate cross-functional, global collaborations and communicate findings to stakeholders, advancing AL amyloidosis programs.

The role requires deep experience in designing multicenter trials, regulatory interactions, and adherence to GCP and FDA guidelines.

Qualifications

• Multi-year experience designing clinical trials and drafting US FDA protocols.
• Experience conceptualizing, designing and conducting complex global trials in Ph1b to registrational stages.
• Strong knowledge of GCP, FDA regulations and international guidelines.

Responsibilities

• Lead drafting of clinical trial protocols for new indications.
• Support cross-functional and global collaborations to integrate scientific and regulatory input into development programs.
• Interpret and communicate clinical trial data.
• Develop key opinion leaders and present at advisory boards and scientific meetings.
• Identify new clinical research opportunities.

Skills

Clinical trial design

US FDA knowledge

Global trial execution

GCP & regulatory familiarity

IND/BLA experience

Education

MD or equivalent

PhD

PharmD

Bachelor’s or higher degree

Job description

Immix Biopharma is seeking an Associate Director, Clinical Development in Los Angeles to lead protocol drafting for new indications and interpret complex trial data. You will coordinate cross-functional, global collaborations and communicate findings to stakeholders, advancing AL amyloidosis programs.

The role requires deep experience in designing multicenter trials, regulatory interactions, and adherence to GCP and FDA guidelines.