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Chief Science Officer - Antiviral Drug Development

Kimer Med

Nelson, Nelson Region, New Zealand · Full Time

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Experience
Any
Salary
Openings
1
Posted
5 days ago
Work mode
In office
Education
PhD or equivalent
Resume
Required to apply

Where you'll work

Job description

About Kimer Med

Kimer Med is a Nelson-based biotechnology company focused on pioneering a novel category of broad-spectrum antiviral medications with the goal of alleviating the global burden of viral diseases.

Role Overview

We seek a seasoned Chief Science Officer (CSO) to steer our scientific and development roadmap as we transition from lead optimization to preclinical development and scale-up phases. This position balances strategic leadership with active scientific engagement, requiring collaboration with our internal research team and external stakeholders including CROs, academic partners, and manufacturing collaborators.

Key Responsibilities

  • Shaping and implementing R&D strategy spanning discovery, lead optimization, and preclinical stages.
  • Leading daily scientific management of a multidisciplinary team covering virology, cell biology, protein science, assay development, and process scale-up.
  • Establishing rigorous go/no-go evaluation criteria for candidate progression based on clear data benchmarks.
  • Formulating and supervising preclinical study strategies (efficacy, PK/PD, toxicology) aligning to regulatory expectations.
  • Managing external partners by overseeing scopes, protocols, timelines, data integrity, interpretation, and reporting.
  • Collaborating closely with process development and pilot manufacturing to guarantee consistent material supply and integration of CMC considerations with development goals.
  • Fostering a culture of scientific excellence emphasizing strong experimental design, reproducibility, thorough documentation, and biosafety compliance.
  • Supporting intellectual property management alongside patent counsel through invention documentation and strategic prioritization.
  • Contributing to investor and partner engagements by preparing scientific content, data rooms, handling technical queries, and delivering presentations.
  • Ensuring robust scientific governance involving risk management and quality assurance in conjunction with QA and CMC teams.

Candidate Requirements

  • Doctorate-level qualification (PhD, MD, DVM, or equivalent) in virology, biochemistry, pharmacology, medicine, or a related life sciences discipline.
  • Extensive experience in drug development, notably in areas such as preclinical candidate selection, IND-enabling studies, or early clinical development support.
  • Excellent command of written and spoken English, capable of clear communication with scientific peers, investors, and collaborators.
  • Proven leadership skills with the ability to define direction, prioritize initiatives, mentor team members, and maintain a respectful, cooperative work environment.
  • Strong organizational aptitude, precision, and detail orientation particularly in documentation and decision-making processes.
  • Experience working within PC-2 laboratory environments.
  • Competent at problem solving and delivering impactful outcomes within a fast-paced startup setting.
  • Willingness to travel periodically for meetings with partners, collaborators, and investors.

Preferred Expertise

  • Background in broad-spectrum antiviral drug discovery and development.
  • Experience interacting with regulatory agencies such as FDA, TGA, or Medsafe and translating science into regulatory-compliant plans.
  • Knowledgeable in managing outsourcing relationships including CRO selection, vendor management, and data quality assurance.
  • Understanding of CMC processes including scale-up, formulation, process development, and quality systems, even if not a specialist.
  • Prior involvement in biotech startups or compact teams with high accountability.
  • Demonstrated capacity to implement comprehensive experimental standards and meticulous documentation practices (including ELN and reporting).
  • Experience compiling scientific materials for investor and partner due diligence processes.

Additional Information

Shortlisted candidates will be subject to a pre-employment drug screening and police check. The role is based at Kimer Med's facilities in Annesbrook, Nelson, New Zealand. Applications must include a cover letter along with a CV.

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