Associate Medical Director

Scorpion Therapeutics; San Diego (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

Scorpion Therapeutics is seeking an Associate Medical Director, Clinical Development to provide medical oversight for metabolic and endocrine disorder therapeutics across late-stage clinical programs. The role involves collaboration with internal teams and external partners to ensure safety and regulatory alignment.

Responsibilities include protocol development support, development planning, data review, trial monitoring, and cross-functional CRO oversight.

Qualifications

• MD, DO, PharmD, or equivalent.
• 2-4 years of clinical or research experience, with late-phase (Phase 2/3) trial exposure preferred.
• Familiarity with GCP, regulatory reporting, and clinical data analysis.

Responsibilities

• Assist in protocol development.
• Contribute to clinical development plans.
• Review safety data and regulatory documents (INDs, CSRs).
• Monitor ongoing studies.
• Serve as a medical contact for trial-related inquiries.
• Provide medical input to cross-functional teams and CRO oversight.
• Support regulatory submissions.
• Assist with data presentation for scientific and regulatory meetings.

Skills

Clinical development

Regulatory reporting

Data analysis

Safety monitoring

Education

MD/DO/PharmD or equivalent

Job description

Role

Associate Medical Director, Clinical Development, supporting medical oversight of clinical trials for metabolic and endocrine disorder therapeutics.

Responsibilities

• assist in protocol development
• contribute to clinical development plans
• review safety data and regulatory documents (INDs, CSRs)
• monitor ongoing studies
• serve as a medical contact for trial-related inquiries
• Provide medical input to cross-functional teams and CRO oversight
• support regulatory submissions
• assist with data presentation for scientific and regulatory meetings

Qualifications

• MD, DO, PharmD, or equivalent
• 2-4 years of clinical or research experience, with late-phase (Phase 2/3) trial exposure preferred
• familiarity with GCP, regulatory reporting, and clinical data analysis

High-Value

expertise in metabolic/endocrine disorders, late-stage clinical development, regulatory documentation, and global safety standards.

WorkSetup

unspecified, with an emphasis on collaboration with internal teams and external partners.