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Arevna

Senior Medical Director

Arevna, Los Angeles, California, United States, 90079

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3 days ago Be among the first 25 applicants This range is provided by Arevna. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range

$300,000.00/yr - $350,000.00/yr Direct message the job poster from Arevna A high-growth, mission-driven biologics company is seeking a Medical Director (or Senior Medical Director, depending on experience) to lead medical strategy and clinical oversight for its expanding development pipeline. This role will be central to shaping study design, ensuring patient safety, and delivering high-quality, compliant clinical trials from concept through completion. As the medical lead for assigned programs, you will collaborate cross-functionally with regulatory, clinical operations, biostatistics, and CMC teams to advance innovative therapies from early development through late-stage trials, supporting the companys mission to improve patient outcomes. Key Responsibilities Serve as medical lead for assigned clinical trials from protocol development to final study report Partner with program management and functional leads to design and execute clinical strategies Provide medical oversight, safety monitoring, and guidance to investigators and study staff Author/review protocols, investigator brochures, informed consent forms, and clinical sections of regulatory submissions Interpret and communicate clinical data to internal stakeholders, regulatory bodies, and external audiences Contribute to Clinical Development Plans (CDPs) and Target Product Profiles (TPPs) Engage with KOLs, advisory boards, patient groups, and regulatory authorities Represent the company at scientific and medical conferences What Were Looking For MD or DO degree; board certification in Endocrinology preferred 4+ years pharmaceutical/biotech clinical development experience for Medical Director level; 5+ years for Senior Medical Director Proven leadership in early- and late-stage clinical programs Strong knowledge of GCP, clinical trial design, and regulatory requirements Excellent communication, scientific writing, and cross-functional leadership skills Ability to thrive in a fast-paced, collaborative, mission-driven environment Why Join? Play a pivotal role in shaping the clinical success of a rapidly growing biologics portfolio Work with an innovative team committed to advancing science-led solutions for patient care Seniority level

Seniority level

Director Employment type

Employment type

Full-time Job function

Job function

Science Industries

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