Level

Generate Biomedicines

Senior Director, Medical Monitor (Respiratory indications)

Generate Biomedicines is hiring a Senior Director, Medical Monitor (Respiratory indications) for a remote role open to applicants in United States. It pays $277k-$416k a year and Level rates it ; you can apply on Generate Biomedicines.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • This is listed as a remote role.
  • The posting mentions clinical trials, medical monitoring and regulatory compliance among its tools and skills.
  • Level classes it as a senior role.
  • Generate Biomedicines has 19 other open roles on Level.

AI in this role

Provide medical oversight and ensure patient safety for late-stage clinical trials in respiratory indications.

clinical-trialsmedical-monitoringregulatory-compliancerespiratory-medicine

The Role:

Generate:Biomedicines 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:Biomedicines, you'll join a mission-driven team committed to scientific excellence!

About Generate:Biomedicines

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:Biomedicines, 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:Biomedicines 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:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines 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 Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto.

 

 

#LI-RT1

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

How we rate this

Senior Director, Medical Monitor (Respiratory indications) at Generate Biomedicines rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Clinical TrialsMedical MonitoringRegulatory ComplianceRespiratory Medicine

Questions you could be asked

  1. Tell me about a project where clinical trials was part of your work. What did you do?
  2. Tell me about a project where medical monitoring was part of your work. What did you do?
  3. Tell me about a project where regulatory compliance was part of your work. What did you do?
  4. Tell me about a project where respiratory medicine was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Clinical Trials, Medical Monitoring, Regulatory Compliance, and Respiratory Medicine. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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