Direct message the job poster from Transpharmation Ltd.
This lab-based role will be to support in vivo models of Pain, cognition and epilepsy for preclinical research studies for our client biotech or pharma companies.
Responsibilities:
* 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 fails.
* Uses 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.
Teamwork and building relationships:
* Be an effective, collaborative hands-on member of the in vivo team, contributing to the overall work of the team as required.
Drive and initiative:
* Plans day to day tasks which will generally be reviewed and approved by supervisor.
* Interprets results and makes decisions with support of supervisor on next steps and approaches.
* Identifies and begins to anticipate, interpret and troubleshoot problems in experimental processes and/or results.
Judgement and problem solving:
* Under supervision, plans and executes a range of study experiments based on established protocols and agreed study design, with clear instructions.
* 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.
* Has a good understanding of the science of the relevant disease models.
* 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.
* Working to the study guidelines without deviation.
* Uses the appropriate statistics and analysis package agreed for that study/model.
* Ensures data integrity is maintained through the correct, prescriptive procedure of logging client data.
Additional benefits:
* Workplace pension with company contribution of 4%
* Life Assurance
* SimplyHealth Cash plan
Seniority level
* Entry level
Employment type
* Full-time
Job function
* Research, Analyst, and Information Technology
* Industries: Research Services
#J-18808-Ljbffr