Associate Medical Director – Medical Director

🕒 September 10

🇺🇸 United States – Remote

💵 $216k - $310k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Iambic Therapeutics

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2019

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

💰 Series B on 2024-04

Healthcare • Consulting • Manufacturing

Iambic Therapeutics is a pioneering biotechnology company that leverages advanced AI algorithms for drug discovery. Their innovative, high-throughput experimental platform aims to address unmet patient needs by optimizing molecules for various therapeutic targets. The company's AI-driven approach allows it to rapidly explore chemical spaces, revealing novel drug mechanisms and delivering high-quality leads at an accelerated pace compared to traditional methods.

📋 Description

• Serve as medical monitor for assigned clinical trials throughout the study lifecycle • Provide medical and scientific expertise for clinical trial execution and oversight • Ensure patient safety, regulatory compliance, and scientific integrity • Review adverse events, serious adverse events, and protocol deviations • Collaborate with pharmacovigilance to assess safety signals • Provide guidance on patient eligibility and protocol adherence • Prepare study protocols, amendments, Investigator Brochures, informed consent forms, and clinical study reports • Review and interpret clinical trial data for safety, efficacy, and accuracy • Support regulatory agency interactions, submission documents, and regulatory meetings • Establish strategic partnerships with KOLs, centers of excellence, and patient advocacy organizations • Develop content for advisory board meetings • Prepare abstracts, scientific symposium presentations, and manuscripts for peer-reviewed journals • Monitor standards of care and experimental therapies through literature and professional meetings

🎯 Requirements

• MD or PharmD with clinical oncology experience and experience in biotech/pharma oncology drug development preferred • PhD with a minimum of 3 years of biotech or pharmaceutical experience in oncology drug development • Experience as a medical monitor on a clinical trial, including patient eligibility review, site interaction to oversee protocol adherence, protocol deviation review, clinical data review and cleaning activities, and coding • Experience executing clinical studies, including interactions with regulatory agencies • Excellent written and verbal communication skills • Ability to work effectively in cross-functional teams with internal and external partners • Excellent organizational and time management skills with strong attention to detail • Proven ability to handle multiple tasks efficiently and effectively • Creative problem-solving skills with proven ability to act proactively • Currently authorized to work in the United States • Must not require visa sponsorship now or in the future

🏖️ Benefits

• Company-paid healthcare • Flexible spending accounts • Voluntary life insurance • 401K matching • Uncapped vacation • Onsite gym • Onsite dining • Brand-new state-of-the-art facility • Easy access to great places to live and play