In Vivo Toxicologist

at  ICON

Reading, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate12 Feb, 2025Not Specified12 Nov, 2024N/ADevelopment Work,Pharmacology,Scientific Background,Toxicology,Project Management SkillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

UK-based In Vivo Toxicologist. Home based, United Kingdom.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.
You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Here in the ICON Strategic Solutions team, we are in an established partnership with a primary multinational pharmaceutical and biotechnology company to supply a full-time, 12-month Fixed-term (with likelihood of extension) UK-based In-Vivo Toxicology Manager to provide leadership and manage study monitors within the client’s Toxicology team. It is a fully home-based role – with no expectation to visit a lab environment.

Responsibilities:

  • MS or BS in Pharmacology, Toxicology or a related Natural Science subject area.
  • Safety assessment experience from non-clinical research and development work within the pharmaceutical and/or CRO industry.
  • Experienced in vivo toxicologist with hands on experience working as either a GLP Study Director and/or Study Monitor for in vivo non-clinical toxicology studies.
  • Good command of pharmacological and/or toxicological principles and methods and the ability to rapidly familiarise with new therapeutic approaches.
  • Familiarity with, and the application of, appropriate regulatory principles and guidelines and the passion to work within and contribute to the subject area of Toxicology in a drug development setting


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

Proficient

1

Reading, United Kingdom