Sr. Medical Director

Meet Life Sciences Ltd.; San Francisco (CA); Hybrid; USD 320,000 - 355,000; Full time

Benefits offered by this job

Bonus

Stock options

Benefits package

Job summary

Meet Life Sciences Ltd. seeks a physician-scientist to lead the medical aspects of autoimmune disease trials, ensuring safety, efficacy, and data integrity. You will design studies, analyze data, and support regulatory submissions while partnering with investigators and sponsors.

The role offers flexible options for remote or hybrid work with potential site travel, requiring strong clinical data interpretation and regulatory knowledge for successful trial execution.

Qualifications

• MD/DO (or equivalent) required with substantial clinical research background.
• 5+ years in clinical research, including 3+ years in late-phase development.
• Experience with autoimmune diseases, neurology, rheumatology, or nephrology preferred.
• Industry experience in cell therapies or related areas desirable.
• Strong ability to interpret and present clinical data with GCP/ICH familiarity.

Responsibilities

• Lead medical monitoring of autoimmune disease trials and engage with investigators.
• Collaborate cross-functionally with clinical operations, biometrics, regulatory and commercial teams.
• Support development of protocols, investigator brochures, and regulatory documents.
• Oversee safety, efficacy, PK, and biomarker data analysis for trial integrity.
• Contribute to regulatory submissions by preparing clinical sections and responses.
• Foster external research collaborations with investigators and sponsors.

Skills

Clinical research experience

Late-phase development

Regulatory knowledge (GCP/ICH)

Data interpretation & presentation

Communication & partnerships

Education

MD/DO (or equivalent)

Job description

Role Summary

You will lead the medical aspects of clinical trials focused on autoimmune disease indications, ensuring the highest standards of safety, efficacy, and scientific integrity. You’ll play a key role in designing studies, analyzing data, and supporting regulatory submissions, all while fostering strong relationships with investigators and research partners. This position offers flexible options for remote or hybrid work, with potential travel to site locations as needed.

Key Responsibilities

• Lead the medical monitoring of clinical trials, engaging with investigators and external medical monitors.
• Manage cross-functional collaboration with clinical operations, biometrics, regulatory, and commercial teams.
• Support the development of clinical trial protocols, investigator brochures, and regulatory documentation.
• Oversee safety, efficacy, PK, and biomarker data analysis to ensure trial integrity.
• Contribute to regulatory submissions by developing and reviewing clinical sections of dossiers and responses.
• Foster external research collaborations through active engagement with investigators and sponsors.

Experience & Qualifications

• MD or DO (or equivalent), with 5+ years of clinical research experience, including 3+ years in late-phase development.
• Strong background in autoimmune diseases, neurology, rheumatology, or nephrology is preferred.
• Industry experience in clinical development of cell therapies or related areas is highly desirable.
• Proven skill in interpreting and presenting clinical data, with familiarity in GCP/ICH and regulatory protocols.
• Excellent communication skills and ability to build effective partnerships with investigators, CROs, and internal teams.

Salary

This role offers a base salary between $320,000 and $355,000 USD, depending on experience, plus bonus, benefits, and stock options.