Senior Director, Medical Monitor (Respiratory indications)
Company shown to members 🔒 · Remote · US only
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First recorded by Psst: 12 October 2026. Your first 3 jobs are free to apply to (the first right away, 2 more with your email). After that, the company and the apply link are for Psst members, from $4.99 for 7 days.
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The 20-second read
- Experience
- 8+ years required
- Where you can live
- US only
- Skills and tools
- machine learning, compliance
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Job details
- Where you can work
- United States
- Employment type
- Not stated by the employer
- Advertised pay
- $277K–416K/yr
- Experience
- 8+ years required
- Employer publication date
- 3 September 2026
- First recorded by Psst
- 12 October 2026
- Last checked at the source
- 10 November 2026
About the job
The Role
Generate:the company is seeking an experienced physician for medical oversight of our late-stage Respiratory (asthma and COPD) programs. This individual will report to the Executive Director of Clinical Development and serve as the Senior Director Medical Monitor for Ph3 global trials, ensuring scientific rigor, patient safety, and executional excellence. The ideal candidate is an MD with deep respiratory expertise and a passion for transforming asthma and COPD care with innovative biologics.
Here's how you will contribute
- Provide day-to day medical oversight for late-stage clinical trials in asthma and/or COPD ensuring patient safety, protocol compliance, data integrity and inspection readiness
- Serve as primary medical contact for clinical sites, investigators, and CROs Perform subject eligibility review, ongoing data reviews, manage study queries, identify and assess protocol deviations
- Serve as a member of the Clinical Development, Safety Management and Study Execution teams
- Contributing author and key reviewer of core clinical and regulatory documents including IB, ICF, RFI, study protocols, DSUR
- Support study oversight committees including DSMB, endpoint adjudication committee, etc.Collaborate cross-functionally with Clinical Operations, Regulatory, Biostatistics, and Pharmacovigilance
- Interpret clinical trial data and contribute to study reports, regulatory filings, and publications
Leadership Responsibilities
- Hold teams to high standards for technical and collaborative performance
- Foster a high-performing, diverse, and inclusive team culture
- Promote enterprise thinking and strategic alignment across functions
- Communicate with clarity, courage, and empathy
- Model resilience, adaptability, and informed risk-taking
The Ideal Candidate will have
- MD (required); board certification in Pulmonology or Allergy & Immunology preferred
- 8+ years of clinical development experience in the biopharma industry
- Extensive expertise in asthma and respiratory clinical trial design, oversight, and execution
- Strong cross-functional leadership and communication skills
- Proven ability to collaborate with internal teams and external stakeholders
Education MD required; additional scientific training (e.g., fellowship, MPH) a plus
Nice to Have
- Experience in both large pharma and biotech settings
- Familiarity with global regulatory frameworks (e.g., FDA, EMA)
- Prior involvement in successful BLA or MAA submissions
Who Will Love This Job
This is an exciting opportunity to shape the future of asthma care by advancing novel biologics using the power of generative biology. At Generate:the company, you'll join a mission-driven team committed to scientific excellence!
About Generate:the company
We are a clinical-stage generative biology company pioneering the AI revolution in drug design and development. We are advancing a new approach to drug creation—one grounded in the ability to design proteins with defined biological intent. By integrating machine learning with large-scale experimentation, this approach aims to reduce the uncertainty, time, and cost associated with developing protein-based medicines.
Founded in 2018, we are advancing a growing pipeline of clinical and preclinical programs across multiple disease areas and protein modalities. By unifying computational design and clinical development within a single operating model, we translate this approach into clinical-stage programs and are leading a shift from traditional drug discovery toward systematic drug generation.
At Generate:the company, we collaborate across disciplines in new ways to invent and innovate. We bring diverse perspectives to a shared goal of delivering better medicines to patients in need, faster, guided by our values and leadership behaviors.
Generate:the company is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Recruitment & Staffing Agencies : Generate:the company does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:the company or its employees is strictly prohibited unless contacted directly by the Company’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of the company:the company and the Company will not owe any referral or other fees with respect thereto.
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Compensation: The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.
Per Year Salary Range
$277,000 — $416,000 USD
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