This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
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.
#J-18808-Ljbffr
Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.