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Crescent Biopharma

Clinical-stage biotech developing solid-tumor therapies

Vice President

Biology & BiotechConfirmed live in the last 24 hours
Full-timeWaltham, MA, USA

About the Job

Requirements

  • Experience leading cross-functional teams in Phase 1–3 drug development is required, and oncology experience is required.
  • An advanced degree in Medical or Life Science, an MD, PhD, or MBA, or equivalent is required.
  • A minimum of 12 years of pharmaceutical-industry experience in leadership positions in drug development with a proven track record driving programs through IND, early clinical, pivotal stages, and approval; alternatively, at least 12 years in significant development and/or commercial leadership or general management positions, including work with development teams in a cross-functional setting, is required.
  • A track record of delivering business objectives and activities or milestones leading to filing and launching, and strong knowledge of oncology, are required.
  • The candidate should be an entrepreneurial team leader able to shape and communicate the vision for a therapeutic program and guide the development and execution of product strategy.
  • Demonstrated experience building effective and motivated cross-functional teams and guiding teams and organizations through complex, high-stakes, data-driven decisions is required.
  • The candidate must be able to pace team work toward milestones in a highly competitive landscape.
  • Strong verbal, written, and presentation communication skills, including the ability to communicate complex ideas clearly to stakeholders and teams at all levels, are required.

Responsibilities

  • Lead a high-performing cross-functional Program Team, focusing on strategy, priorities, output, resources, and building a fulfilling, collaborative, and sustainable team environment.
  • Establish a robust, well-understood Program strategy for bringing a medicine to patients in need.
  • Ensure research, non-clinical, clinical, regulatory, CMC, and commercial strategies and plans align with the overall Program strategy.
  • Structure and facilitate critical cross-functional decisions within the Program Team and senior leadership team, considering relevant perspectives and driving efficient decisions.
  • Own Program recommendations across stages to achieve milestones and timelines.
  • Drive preparation and presentation of materials for the Board of Directors.
  • Communicate proactively with senior leadership and stakeholders about Program strategy, status, priorities, risks, and needs, and facilitate appropriate decision-making.
  • Monitor emerging developments, external non-clinical and clinical data updates, and competitive intelligence in oncology, and ensure learnings and implications are communicated and reflected in internal Program plans.
  • Build a visible, constructive, and credible presence within relevant disease-area key opinion leader and patient communities.
  • Participate in business development activities as needed, including opportunity evaluations and due diligence.
  • Foster collaboration, innovation, discovery, scientific excellence, open communication, and continual improvement in R&D.
  • Coach team members to achieve their best and support them in mitigating skill or capacity gaps.
  • Consider Program needs in the context of corporate strategy and priorities, and advocate for the Program among senior leadership.
  • Lead in accordance with Crescent’s core values.

Desired Qualifications

  • Experience with antibody-drug conjugates (ADCs) is a plus.

About the Company

Crescent Biopharma

Clinical-stage biotech developing solid-tumor therapies

Crescent Biopharma develops oncology therapies for solid tumors, led by CR-001, a tetravalent bispecific antibody that blocks PD-1 and VEGF to boost anti-tumor immunity while inhibiting tumor blood vessel growth. CR-001 sits in a global Phase 1/2 ASCEND trial, and the pipeline also includes CR-002, an anti-PD-L1 antibody-drug conjugate, and CR-003, an ITGB6-targeted ADC. The company differentiates itself by combining immune checkpoint blockade with VEGF inhibition and other targeted modalities to build an immuno-oncology backbone for solid tumors, supported by strategic partnerships and substantial private placements. Crescent’s goal is to advance multi-agent regimens toward regulatory approval and commercial development for patients with solid tumors.

Company size
51-200
Company stage
IPO
Headquarters
Waltham, MA
Founded
2003

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