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Vivo Consulting is seeking a motivated in vivo pharmacology specialist with expertise in rodent studies to support in vivo models for preclinical research. This lab-based role partners with our client biotech or pharma companies.
You will plan and perform in vivo preclinical studies, generate protocols, maintain records, and ensure regulatory and safety standards are met. A team-oriented role with independence in a fast-paced environment.
A motivated and pro-active in vivo pharmacology individual with expertise in in vivo studies, specifically rodent studies.
This lab-based role supports in vivo models for preclinical research studies for our client biotech or pharma companies.
Planning and hands-on execution of in vivo preclinical studies
Generating high-quality protocols/study plans and carrying out client study requests within agreed timelines.
Generating and maintaining clear experimental records
Good data entry skills and interpretation of the results, ability to communicate results via informal discussions
Has a good understanding of the science of the relevant disease models
Be an effective, collaborative hands-on member of the in vivo team, contributing to the overall work of the team as required
Ensuring appropriate use of animals in compliance with all regulatory requirements and internal standards
Ensuring all Standard Operating Procedures, Health and Safety and regulatory requirements are adhered to
Using best judgment to carry out work to the highest standard
Excellent organisational, problem-solving and communication skills
Ability to work well within a team, as well as independentlyand proactively
Ability to work on multiple studies in multiple areas in a fast-paced environment
Highly motivated and ability to be flexible in case of changing priorities.
Responsible for timely, accurate recording of results.
Ensures data integrity is maintained through the correct, prescriptive procedure of logging client data.
Produces high standard, good quality data to provide to clients, reproducible, without fail.
Use standard established statistical and analysis packages.
Supports data entry and study documentation in relation to ethics and welfare.
May start to present results in lab meetings.
Consults with supervisor when difficulties arise that cannot be readily resolved.
Seeks input as needed from supervisor or other scientific staff for guidance
Communicates and collaborates with scientific staff
Reports study deviations to line manager promptly to protect company and client interests
Good data entry skills and interpretation of the results, ability to communicate results via informal discussions
Generating and maintaining clear experimental records
May interact with clients when required, effectively maintaining and building working relationships
BSc degree with significant relevant lab-based experience, preferably in the pharmaceutical or biotechnology industry or a similar HNC in Biology, Pharmacology, Neuroscience, or a related discipline.
HO licence 1-4, including rodent dosing, behavioural testing, surgical techniques, tissue dissections
Ability to manage data entry, and data recording, some experience in analysing data and report writing
Excellent organisational, problem-solving and communication skills
Ability to work well within a team, as well as independently and proactively
Ability to work on multiple studies in multiple areas in a fast-paced environment
Highly motivated and ability to be flexible in case of changing priorities.