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Forbion

Vice President Research and Development

Translational Research & Bench BiologyConfirmed live in the last 24 hours
Full-timeNaarden, NetherlandsNo salary listedIn-person

About the Job

Requirements

  • A PhD, MD/PhD, or equivalent advanced scientific training in immunology, tumour immunology, molecular/cell biology, pharmacology, or a related discipline.
  • Approximately 15 or more years of relevant research and development experience in biotech and/or biopharma.
  • Deep expertise in immunology, ideally spanning human immunology, immune-mediated disease, inflammation, and/or tumour immunology.
  • Demonstrated experience progressing therapeutic programmes through candidate selection and IND-enabling development.
  • Strong translational-science capability across human biology, biomarkers, pharmacokinetics/pharmacodynamics, target engagement, pharmacology, and clinically relevant models.
  • Experience designing and interpreting in vitro, ex vivo, and in vivo studies supporting therapeutic development.
  • Working knowledge of nonclinical safety, toxicology, bioanalytics, and regulatory requirements associated with IND/CTA submissions.
  • Significant experience managing contract research organizations and specialist external partners through defined study objectives, decision criteria, timelines, and budgets.
  • Strong programme and portfolio judgement, including the ability to make difficult stop/go decisions based on incomplete or evolving datasets.
  • A demonstrated ability to lead, motivate, and develop high-calibre scientific teams.
  • Exceptional communication skills and comfort operating from detailed scientific discussion through to executive and Board-level dialogue.

Responsibilities

  • Provide scientific and strategic leadership for programmes progressing from discovery through candidate selection, preclinical development, and IND-enabling activities.
  • Partner closely with Discovery leadership to ensure programmes transition with clear target product profiles, biological rationale, and development plans.
  • Establish rigorous translational strategies integrating mechanism of action, pharmacology, pharmacokinetics/pharmacodynamics, biomarkers, target engagement, efficacy, safety, and clinically relevant models.
  • Ensure programmes are designed from an early stage with human translation and clinical differentiation in mind.
  • Identify critical scientific questions and development risks early, ensuring experiments generate decisive and actionable data.
  • Maintain a high bar for scientific quality while balancing depth of investigation with the pace and pragmatism required in biotech.
  • Provide appropriate scientific input to IND-enabling packages and regulatory submissions alongside relevant internal and external specialists.
  • Lead and develop Project Science Leads, establishing clear accountability for scientific strategy and programme delivery.
  • Drive cross-functional teams against clearly defined milestones, timelines, decision points, and stage gates.
  • Establish robust programme plans from discovery through development-candidate nomination and IND-enabling development.
  • Challenge programme assumptions constructively and ensure key decisions are grounded in high-quality evidence.
  • Identify scientific, translational, and execution risks early and develop pragmatic mitigation plans.
  • Work with the CSO and Research Leadership Team on portfolio prioritisation, resource allocation, and investment decisions.
  • Create transparency around programme progress, critical-path activities, and key scientific decisions.
  • Own scientific relationships with key contract research organizations and external research partners supporting preclinical development.
  • Determine which capabilities should be accessed externally and select partners based on scientific quality, speed, technical fit, and value.
  • Ensure external studies are appropriately designed, commissioned, monitored, and interpreted.
  • Hold external partners accountable for agreed scientific quality, timelines, budget, and deliverables.
  • Ensure knowledge, interpretation, and decision-making remain firmly owned internally when execution is outsourced.
  • Act as a close scientific and operational partner to the CSO across the research and development portfolio.
  • Help drive activity, priorities, and follow-through across the Research Leadership Team.
  • Distil complex scientific information into clear options, risks, and recommendations for executive decision-making.
  • Prepare high-quality scientific materials for senior leadership, the Board, partners, and external stakeholders.
  • Support strategic diligence, collaboration discussions, and scientific evaluation of external opportunities where relevant.
  • Represent the company’s science credibly with partners, advisors, key opinion leaders, and at scientific meetings.

Desired Qualifications

  • Experience across more than one relevant biotech and/or pharmaceutical environment.

About the Company

Company size
Not listed
Company stage
Not listed
Total funding
$11.6B
Headquarters
Naarden, Netherlands
Founded
2006

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