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Toxicologist / Study Director- Gene Therapy

LondonPermanent
Experience Dependent
Job Reference: J5635532
Updated On: 06/10/2021
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Biotechnology, Cell & Gene Therapy

Skills: Pharmacology - In Vivo, Toxicology - Pharma

Job Information

Role Overview

HRS are currently looking for a Toxicologist - Gene Therapy to join a leading gene therapy company based in London. As the Toxicologist - Gene Therapy you will be responsible for coordinating non-clinical studies focused on GLP safety / toxicology studies as well as support with regulatory submissions for clinical trial approval.

This is a great opportunity for an experienced toxicologist / study director from a CRO and/or Pharma background who is keen to join an innovative organisation that supports in the development of gene therapies for rare diseases.

For this role you will require to be on site 4 days a week.

Key Duties and Responsibilities

Your duties as the Toxicologist - Gene Therapy will be varied however the key duties and responsibilities are as follows:

1. You will be responsible for vendor selection, protocol preparation, study initiation and oversight of GLP non clinical outsourced safety studies.

2. In this role you will write, review, edit study protocols and reports for regulatory submissions.

3. You will manage the studies from start to finish ans ensure all timelines are met and all actions required followed up.

4. As the Toxicologist - Gene Therapy, you will oversee the development and qualification of assays required for sample analysis within safety studies.

Role Requirements

To be successful in your application to this exciting opportunity as the Toxicologist - Gene Therapy we are looking to identify the following on your profile and past history:

1. Relevant degree in a MSc or PhD in toxicology, biochemistry pharmacology or other scientific discipline.

2. Proven industry experience in managing non clinical in vivo GLP safety / toxicology studies within a CRO or Pharmaceutical company.

3. A working knowledge and practical experience with GLP toxicity requirements across EU / USA.

Key Words: Toxicology / Toxicologist / Non Clinical / GLP / In Vivo GLP / Safety Studies / Toxicology Studies / Study Manager / Study Director / Gene Therapy / Biotech / Londo
Christina Giakou
Your Recruitment ConsultantChristina GiakouChristina.giakou@hyperec.com
DisclaimerHyper 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.