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Consultant Call - Preclinical pharmacology consultant (Peptide Therapeutics)

Constructive Bio

Cambridgeshire and Peterborough
Remote
GBP 80,000 - 100,000
26 days ago
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Portfolio Strategy Manager (UK Remote)

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GBP 60,000 - 80,000
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Mortgage Advisor / Life & Protection Adviser / Broker in Sunderland)

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Consultant Call - Preclinical pharmacology consultant (Peptide Therapeutics)
Constructive Bio
Cambridgeshire and Peterborough
Remote
GBP 80,000 - 100,000
Part time
26 days ago

Job summary

A biotechnology firm is seeking an experienced DMPK consultant to support peptide therapeutic development. Responsibilities include planning in vivo/in vitro studies, advising on DMPK strategy, and analyzing data. The ideal candidate has a proven track record in DMPK for peptides or biologics and is available for short- or medium-term consulting. Strong communication skills are essential.

Qualifications

  • Track record in DMPK for peptides or biologics.
  • Experience with PK/PD modelling and half-life extension technologies.
  • Ability to provide strategic guidance and hands-on analysis.

Responsibilities

  • Plan and review in vivo studies.
  • Plan and review in vitro assays.
  • Advise on overall DMPK strategy for peptides.
  • Analyze data and recommend next steps.
  • Support vendor/CRO selection and study oversight.

Skills

DMPK expertise for peptides
PK/PD modelling
Strong communication skills
Job description
Overview

Consultant Call - DMPK (Peptide Therapeutics). Constructive Bio is seeking an experienced DMPK or PK/PD (preclinical pharmacology) consultant to support ASAP the design and delivery of our peptide development programs. Our pipeline includes engineered peptides incorporating non-canonical amino acids, and we need expertise to translate molecular design into clear DMPK strategies and data packages. We need someone experienced available now. We are open to short- or medium-term consulting arrangements.

Responsibilities
  • Plan and review in vivo studies (PK, bioavailability, half-life, clearance routes, immunogenicity considerations).
  • Plan and review in vitro assays (plasma stability, protease resistance, plasma protein binding, permeability).
  • Advise on overall DMPK strategy for peptides, including study design, interpretation, and regulatory expectations.
  • Analyse data, highlight risks, and recommend next steps to guide project teams.
  • Benchmark against industry best practices and prepare input suitable for preclinical packages.
  • Support vendor/CRO selection and study oversight.
Requirements
  • Track record in DMPK for peptides or biologics, ideally in pharma/biotech. Evidence for the track record needs to be provided.
  • Experience with PK/PD modelling, half-life extension technologies, and translation from animal to human.
  • Ability to work flexibly as a consultant, providing both strategic guidance and hands-on analysis.
  • Strong communication skills to work with internal scientists and external partners.
Desirable
  • Experience of in vitro and in vivo safety and toxicology studies
  • Knowledge and preparation of IND documents would be an advantage
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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