Chief Science Officer - Antiviral Drug Development
Nelson, Nelson Region, New Zealand · Full Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 4 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.