Parabilis Medicines logo
Parabilis Medicines

Advancing ultra-tunable Helicon peptide therapeutics to achieve extraordinary outcomes for people affected by cancer.

Senior Director, Clinical Sciences

DirectorDirectorFull TimeRemoteLeadTeam 51-200Since 2016H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

36 days ago

Salary

$265K - $305K / year

Seniority

Lead

No structured requirement data.

Job Description

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more.

Role Description

Parabilis Medicines is seeking a Senior Director, Clinical Sciences to provide scientific and strategic leadership across our clinical development programs. This role is central to translating discovery and preclinical innovation into high-quality, data-driven clinical development strategies that advance our pipeline efficiently and responsibly.

As Senior Director, Clinical Sciences, you will:

  • Lead and own clinical science strategy for one or more clinical programs across development stages
  • Drive scientific input into protocol design, endpoint selection, and clinical development plans
  • Serve as a core contributor to regulatory interactions, governance decisions, and program reviews
  • Influence portfolio strategy through integrated clinical and translational insights
  • Partner closely with Clinical Operations to ensure scientifically sound and feasible trial execution
  • Interpret and contextualize clinical, biomarker, and safety data to inform decision-making
  • Contribute to regulatory documents (INDs, IBs, briefing packages) and regulatory interactions
  • Support investigator meetings, advisory boards, and external scientific communications
  • Ensure consistency of scientific messaging across internal and external stakeholders
  • Mentor and guide junior clinical scientists as the organization grows
  • Leverage AI-enabled tools to enhance clinical insights, literature analysis, data interpretation, and operational efficiency

Qualifications

  • PhD, PharmD, or equivalent advanced degree in life sciences, medicine, or a related field
  • 10+ years of experience in clinical development or clinical sciences within biotech or pharmaceutical settings
  • Direct experience supporting or leading clinical trials (Phase 1–3 preferred)
  • Proven track record of contributing to successful clinical programs and regulatory milestones
  • Deep understanding of clinical trial design, endpoints, and regulatory requirements
  • Experience working with clinical data systems, trial databases, and scientific literature platforms
  • Familiarity with biomarker and translational data integration
  • Strong scientific writing and data presentation skills
  • Experience in rare disease, oncology, immunology, or other complex therapeutic areas (as applicable to Parabilis’ pipeline)
  • Prior leadership or matrix-management experience
  • Experience interacting with regulatory agencies and external experts
  • Strong strategic thinking combined with hands-on execution
  • Comfort operating in a fast-paced, evolving biotech environment
  • Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.

Benefits

  • Base salary range: $265,000–$305,000 per year, depending on experience, qualifications, and internal practices
  • Annual target bonus
  • Equity
  • Comprehensive suite of competitive benefits designed to support employees’ overall well-being

Core Values

  • Growth-Minded: We’re inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.
  • In(ter)dependent: We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.
  • Patient-focused: We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.
  • All-In: We’re All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

Job Requirements

  • PhD, PharmD, or equivalent advanced degree in life sciences, medicine, or a related field
  • 10+ years of experience in clinical development or clinical sciences within biotech or pharmaceutical settings
  • Direct experience supporting or leading clinical trials (Phase 1–3 preferred)
  • Proven track record of contributing to successful clinical programs and regulatory milestones
  • Deep understanding of clinical trial design, endpoints, and regulatory requirements
  • Experience working with clinical data systems, trial databases, and scientific literature platforms
  • Familiarity with biomarker and translational data integration
  • Strong scientific writing and data presentation skills
  • Experience in rare disease, oncology, immunology, or other complex therapeutic areas (as applicable to Parabilis’ pipeline)
  • Prior leadership or matrix-management experience
  • Experience interacting with regulatory agencies and external experts
  • Strong strategic thinking combined with hands-on execution
  • Comfort operating in a fast-paced, evolving biotech environment
  • Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.

Benefits

  • Base salary range: $265,000–$305,000 per year, depending on experience, qualifications, and internal practices
  • Annual target bonus
  • Equity
  • Comprehensive suite of competitive benefits designed to support employees’ overall well-being
  • Core Values
  • Growth-Minded: We’re inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.
  • In(ter)dependent: We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.
  • Patient-focused: We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.
  • All-In: We’re All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

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