Logo for Faeth Therapeutics

Senior Medical Director

Role overview

Qualifications

  • M.D. degree or PA/NP/PhD
  • 2+ years as a clinical scientist or medical director in the biotech or pharmaceutical industry
  • Prior experience serving as a Medical Monitor for interventional clinical trials
  • Strong communication, ownership and decision-making skills

Responsibilities

  • Serve as the primary Medical Monitor for assigned clinical trials
  • Provide ongoing medical oversight to ensure patient safety and protocol compliance
  • Lead ongoing clinical data review to ensure integrity, completeness, and scientific validity
  • Provide strategic guidance across functions to optimize trial design, recruitment, and execution

Key facts

Other skills

  • Communication
  • Decision Making
  • Problem Solving
  • Physical Flexibility

About the company

Faeth Therapeutics logo

Faeth Therapeutics

Biotechnology

Everything needs food to survive and grow, including cancer. There is an entire dimension of human biology in metabolism that’s been too complex to leverage in the fight against cancer––until now.

Company details

IndustryBiotechnology
Company size11 - 50

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. With a strong scientific foundation and a founding team that includes the discoverer of our target pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, toward multiple near-term milestones. We are a small, focused team where every person has direct impact β€” united by a shared commitment to care deeply, create boldly, and never stop learning.

The Senior Medical Director will provide strategic and operational medical leadership across the clinical development lifecycle. This individual will serve as the medical monitor and cross-functional medical lead for assigned programs, ensuring scientific rigor, patient safety, and high-quality data generation while working collaboratively to execute efficiently and successfully. This is a lead role in a small, fast-paced biotech where there will be significant opportunities for creativity, problem-solving and contributing to a range of cross-functional activities. 

Reports to: Chief Medical Officer
Location: Remote (U.S.)

Responsibilities

Medical Monitoring

  • Serve as the primary Medical Monitor for assigned clinical trials.
  • Provide ongoing medical oversight to ensure patient safety and protocol compliance.
  • Review eligibility queries, protocol deviations, and safety data in real time.
  • Collaborate with Safety/Pharmacovigilance on SAE review, signal detection, and benefit-risk assessments.
  • Support investigator communications and training related to medical and safety matters.

Data Review & Quality Oversight

  • Lead ongoing clinical data review to ensure integrity, completeness, and scientific validity.
  • Partner with Clinical Operations and Data Management to ensure high data quality standards.
  • Identify data trends, inconsistencies, and potential safety or efficacy signals.
  • Contribute to statistical analysis planning and interpretation of study results.
  • Ensure readiness for database lock and regulatory submissions.

Cross-Functional Clinical Development Leadership

  • Provide strategic guidance across functions to optimize trial design, recruitment, and execution.
  • Contribute to translational and biomarker strategies 
  • Collaborate cross-functionally on briefing documents, INDs, NDAs/BLAs, and agency interactions.
  • Lead medical communications including abstracts, manuscripts, and congress presentations.

Qualifications

  • M.D. degree or PA/NP/PhD  
  • 2+ years as a clinical scientist or medical director in the biotech or pharmaceutical industry.
  • Prior experience serving as a Medical Monitor for interventional clinical trials.
  • Experience in clinical data review and ensuring data quality.
  • Experience leading cross-functional clinical development teams.
  • Experience with regulatory authority interactions is preferred.
  • Strong communication, ownership and decision-making skills.
  • Common sense and flexibility 

Compensation Range: $325,000 - $400,000 (actual compensation may vary based on experience, qualifications and location)

Working at Faeth

Benefits:

  • Competitive salary and equity in a well-funded, clinical-stage biotech
  • 100% remote work and flexible schedule
  • Health, dental, and vision for you and your dependents
  • Flexible time off
  • Generous parental leave
  • Traditional and Roth 401k 
  • Mission oriented, remote first culture

We are an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

All offers of employment are contingent upon satisfactory completion of a background check and verification of eligibility to work in the United States.

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
Β·

Medical Administrator Related jobs

Other jobs at Faeth Therapeutics

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.