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In Vitro Study Director

Cheshire   •  £30000 - £45000 per annum, Benefits: Yes  •  Permanent, Full time


We are currently looking for a highly motivated Study Director to join a leading genetic toxicology CRO based in the Cheshire area. As the Study Director, you will be responsible for study investigations within the in vitro micronucleus team, researching predictive and preclinical toxicology products and services across a variety of industry sectors.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as a Study Director will be varied however the key duties and responsibilities are as follows:

1. You will be involved with high quality genotoxicity and micronucleus studies where you will be ensuring the you meet study deadlines.

2. As a Study Director, you will be responsible for executing and reporting the preclinical studies.

3. It will be your responsibility to ensure studies are conducted in accordance with approved study plans and in compliance to GLP principals.

4. You will be driven and motivated to maintain the integrity of studies and the products that the CRO works with, while willing to learn and deliver other toxicological assays depending on the workload.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Study Director we are looking to identify the following on your profile and past history:

1. A relevant degree in a life science subject (e.g. Toxicology, Pharmacology, Cell Biology, Genetics, Molecular Biology, etc.) is required.

2. Proven Academic or Industry experience in a life science laboratory performing in vitro toxicology and cell-based assays is necessary, more valuable if within a research or CRO setting. This role is open to those looking to train for an In Vitro Study Director role.

3. A working knowledge and practical experience with genotoxicity and micronucleus tests and a hands-on experience with fluorescence microscopy and cytogenetic techniques will be beneficial.

Key Words: Scientist | Study Investigator | Toxicology | Cytotoxicity | Cytogenetics | Micronucelus | Life Science | GLP | CRO | Assays | Fluorescence Microscopy | In vitro | Automated | Semi-automated | Preclinical | Study Scientist | Study Management | Gene Mutation | OECD | Pharmaceutical | Agrochemical | Predictive Toxicology | Genotoxicity | Genetic Toxicology | North West | Cheshire | Study Director

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.


You must be eligible to work in the UK. Learn more

  • Agency: Hyper Recruitment Solutions
  • Contact: Sarah Audit
  • Phone: 0203 910 2980
  • Reference: J5635263
  • Posted: 13th July 2021
  • Expires: 10th August 2021

Hyper Recruitment Solutions

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