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Open nowPosted 3 days ago

Senior Director, In Vivo Pharmacology

Generate Biomedicines18 open roles

Pay
$219,000 – $300,000 a year
Where
Somerville, MA
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Your applicationOpen nowSenior Director, In Vivo PharmacologyGenerate Biomedicines · Somerville, MA
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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market. Generate Biomedicines postings stay open a median of 28 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.4%3 days
  3. 7.8%7 days
  4. 14.3%14 days
  5. 33.7%30 days
This job: posted 3 days ago

Generate Biomedicines median: 28 days open

The posting

The Role:

Gnerate:Biomedicines is a new kind of therapeutics company at the intersection of machine learning, biological engineering, and medicine, pioneering Generative Biology™ to create breakthrough medicines where novel therapeutics are computationally generated rather than discovered.

We are seeking a Senior Director, In Vivo Pharmacology to provide scientific and organizational leadership for in vivo pharmacology and help advance a growing portfolio of novel biologic medicines from early discovery through development.

Reporting to the Head of Preclinical Pharmacology, this individual will lead and develop a team of in vivo pharmacology scientists while shaping and executing in vivo pharmacology strategies across programs. In close partnership with Preclinical Pharmacology, Early Biology, and other scientific and development functions, the Senior Director will ensure that in vivo studies are tightly connected to mechanistic understanding, in vitro functional and high-throughput data, and emerging translational evidence.

The Senior Director will also work closely with the translational biology function to help establish and incorporate appropriate human experimental systems and New Approach Methodologies (NAMs) into preclinical pharmacology strategies where they can add value. This will complement and inform traditional in vitro and in vivo approaches and help strengthen the connection between preclinical findings and human biology for more informative and successful FIH studies.

This role sits at the intersection of scientific strategy, experimental execution, and organizational leadership. The Senior Director will connect technology and mechanism to pharmacology, pharmacology to translation, and experimental evidence to program decisions. They will work across functions to ensure that pharmacology strategies are rigorous, appropriately quantitative, and aligned with development objectives and regulatory expectations.

The successful candidate will bring deep expertise in in vivo pharmacology and drug development, strong scientific judgment, and a demonstrated track record of building and developing high-performing scientific teams. Equally important, they will thrive in an environment that values scientific rigor, innovation, thoughtful experimentation, collaboration, transparency, and the willingness to challenge conventional approaches in pursuit of better medicines for patients.

Here's how you will contribute:

Scientific and Strategic Leadership

· Provide strategic and scientific leadership for in vivo pharmacology across discovery and development programs, translating program hypotheses into rigorous, decision-enabling experimental strategies.

· Partner with program and functional leaders to develop integrated pharmacology plans encompassing model selection, study design, pharmacodynamic and efficacy endpoints, dose and schedule optimization, and translational strategies.

· Critically evaluate the relevance, strengths, and limitations of in vivo models and develop fit-for-purpose approaches that reflect disease biology, mechanism of action, therapeutic modality, and stage of development.

· Integrate in vivo pharmacology and PK/PD findings with in vitro functional and high-throughput data, translational biology, biomarkers, safety, and other relevant datasets to build a cohesive understanding of therapeutic activity and inform candidate progression.

· Apply strong scientific judgment to complex and ambiguous datasets, identifying key risks, knowledge gaps, and opportunities for experiments or technologies that can efficiently resolve uncertainty.

· Serve as a senior pharmacology partner on cross-functional program teams, influencing program strategy and communicating scientific recommendations clearly to scientific and organizational leadership.

· Ensure that pharmacology strategies evolve with program maturity, from early mechanism and proof-of-concept through candidate selection, IND-enabling studies, and first-in-human development.

· Coach and develop direct reports through regular feedback, career development, scientific mentorship, and opportunities to expand their technical and leadership capabilities, while helping them define and pursue meaningful career paths within the organization.

· Work closely with the translational biology team to help incorporate relevant human experimental systems, including NAMs, when appropriate, and contribute in vivo pharmacology expertise to the development and interpretation of translational strategies.

· Identify opportunities to strengthen the connection between preclinical pharmacology findings and human biology, clinical hypotheses, and development decisions.

Scientific Excellence and Execution

· Drive high standards for experimental design, data quality, reproducibility, documentation, quantitative analysis, and scientific interpretation across internal and external in vivo studies.

· Identify opportunities to expand and evolve Generate's in vivo pharmacology capabilities, including new models, technologies, quantitative approaches, and experimental strategies.

· Establish and oversee productive relationships with CROs and external research partners, ensuring scientific quality, operational excellence, and alignment with program objectives.

· Foster transparent and courageous communication, encouraging the team to surface risks, uncertainties, and differing scientific perspectives early and use evidence to reach well-reasoned decisions.

· Contribute in vivo pharmacology expertise to regulatory and development activities, including the preparation and review of relevant scientific and regulatory documentation.

· Communicate complex scientific findings and recommendations to audiences with varying technical backgrounds, clearly distinguishing evidence, interpretation, uncertainty, and recommended next steps.

Leadership Responsibilities

As Senior Director, In Vivo Pharmacology, you will lead and develop a team of in vivo pharmacology scientists and help build a critical capability within Preclinical Pharmacology. You will have accountability for the team's scientific strategy, performance, capabilities, and development.

· Lead, manage, and develop a high-performing team of scientists responsible for in vivo pharmacology across Generate's portfolio, establishing clear roles, priorities, and expectations.

· Recruit and retain exceptional scientific talent and build the capabilities and expertise required to support both the current portfolio and Generate's evolving scientific needs.

· Set a high bar for scientific rigor, execution, accountability, and collaboration, ensuring that team members understand how their work connects to program, functional, and company objectives.

· Coach and develop direct reports through regular feedback, career development, scientific mentorship, and opportunities to expand their technical and leadership capabilities.

· Develop future leaders within the team and appropriately delegate scientific and organizational ownership, creating an organization that can operate effectively as the portfolio grows.

· Create an inclusive environment in which scientists are empowered to challenge assumptions, debate scientific hypotheses, take thoughtful risks, and learn openly from both successful and unsuccessful experiments.

· Establish effective operating mechanisms for prioritizing resources and studies across programs, balancing portfolio needs, scientific opportunities, team capacity, and timelines.

· Foster the development of scientific talent across the broader Preclinical Pharmacology organization, providing mentorship and sponsorship to early- and mid-career scientists and creating opportunities for them to expand their scientific judgment, technical expertise, visibility, and leadership capabilities.

· Partner with the Head of Preclinical Pharmacology to define functional priorities, evolve capabilities, allocate resources, and ensure that in vivo pharmacology operates as an integrated scientific partner rather than a downstream execution function.

· Collaborate closely with the translational biology leader and other peer functional leaders to ensure effective integration of in vivo pharmacology with broader preclinical and translational strategies.

· Partner with peer leaders across Generate to ensure that the organization is positioned to meet the evolving needs of the portfolio and to build capabilities that scale with the company.

· Model adaptability, accountability, and resilience as programs, hypotheses, and organizational priorities evolve while maintaining a strong commitment to scientific rigor and innovation.

The Ideal Candidate will have:

· PhD in Pharmacology, Biology, Immunology, Oncology, Neuroscience, or a related scientific discipline, with 12+ years of relevant experience in biotechnology or pharmaceutical drug discovery and development, including significant experience leading and developing scientific teams.

· Deep expertise in in vivo pharmacology, with demonstrated experience designing, interpreting, and integrating pharmacology studies that inform drug discovery and development decisions.

· Broad understanding of the relationships among disease biology, mechanism of action, exposure, target engagement, pharmacodynamics, efficacy, and translational relevance.

· Demonstrated ability to develop in vivo strategies for complex therapeutic programs and select fit-for-purpose models based on scientific evidence, mechanism, therapeutic modality, and development objectives.

· Experience advancing therapeutic candidates through key discovery and preclinical development milestones.

· Strong understanding of experimental design, quantitative data interpretation, and the strengths, limitations, and translational relevance of preclinical models.

· Experience across multiple therapeutic modalities; experience with biologics development is highly valuable.

· Demonstrated ability to integrate complex datasets and translate them into clear scientific conclusions, program implications, and actionable recommendations.

· Significant experience leading, managing, and developing scientists in a high-performing, multidisciplinary industry research environment.

· Demonstrated success recruiting talent, setting performance expectations, coaching team members, and developing scientific and leadership capabilities.

· Track record of effective scientific leadership on multidisciplinary drug discovery or development teams.

· Ability to influence decisions across organizational boundaries through scientific credibility, sound judgment, and clear communication.

· Experience managing external research partnerships and CRO relationships.

· Strong written and verbal communication skills, including the ability to present complex scientific information and recommendations to senior scientific and business leaders.

· A collaborative leadership style and demonstrated commitment to scientific rigor, transparency, accountability, and continuous learning.

Nice to Have

· Experience developing pharmacology strategies for novel or emerging biologic modalities.

· Experience contributing to IND-enabling programs and regulatory submissions.

· Expertise in translational pharmacology, PK/PD, biomarkers, or quantitative approaches for connecting preclinical findings with clinical hypotheses.

· Experience establishing or scaling in vivo pharmacology capabilities, platforms, or teams within a growing biotechnology organization.

· Familiarity with human experimental systems, New Approach Methodologies (NAMs), or other approaches that can complement traditional preclinical models.

· Experience using computational, data-driven, or technology-enabled approaches to improve experimental design, model selection, or interpretation of pharmacology data.

· Scientific contributions demonstrated through publications, patents, external presentations, or other evidence of leadership within the field.

Who Will Love This Job:

This is an opportunity to help define how in vivo pharmacology contributes to a fundamentally different approach to creating medicines.

At Generate, computationally generated proteins give us the opportunity to explore therapeutic design space in ways that traditional discovery approaches cannot. Realizing that potential requires equally rigorous experimental science: asking the right biological questions, designing studies that meaningfully test our hypotheses, and integrating diverse datasets to generate insights that can move promising medicines toward patients.

As Senior Director, In Vivo Pharmacology, you will have the opportunity to shape that work at both the scientific and organizational levels. You will build and develop the team and capabilities needed for a growing portfolio, influence programs across stages of discovery and development, and work closely with scientists across Generate to connect in vitro and in vivo pharmacology with broader translational strategies.

We are looking for a leader who is deeply scientific, relentlessly curious, comfortable challenging assumptions, and energized by the opportunity to build a strong, cutting edge in vivo pharmacology capability that helps translate Generate's Generative Biology™ platform into meaningful medicines.

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

$219,000—$300,000 USD

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