Overview
Join to apply for the Clinical Research Assistant role at Eurofins Food & Water Testing UK & IE.
Eurofins Scientific is an international life sciences company, providing a range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. Eurofins laboratories work with the biggest companies in the world to ensure products are safe, ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
We are an armed-forces-friendly employer and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners.
If you want to help make our world a safer and healthier place, apply for the role below and become part of the extraordinary Eurofins.
Job details
35 Hours per week. Monday - Friday. 9.00am - 5.00pm. Please note that visa sponsorship is not available for this role.
Purpose of the post
Responsible for assisting with the delivery of a portfolio of clinical studies including adherence to regulatory processes within the department.
Responsibilities
* To assist & organise research study setup and preparation.
* Assess eligibility of potential volunteers through screening interviews, reviews of medical records, and discussions with the Project Manager.
* Contact volunteers to recruit them for specific studies, schedule visits and perform related administration on the database.
* Provide support to volunteers, study team staff and more senior colleagues.
* Maintain systems and undertake routine tasks that support the working of teams, processes and/or studies.
* Ensure relevant documents are available for all research subjects.
* Complete all documentation relating to volunteer participation, including database demographic data records, Case Report Forms (CRFs) and electronic research records.
* Handle telephone enquiries from volunteers, external and internal customers.
* Interact with study participants in relation to study requirements.
* Ensure test materials and other consumables are available for study commencement and that disposal is carried out on study completion.
* Dispense and prepare study test materials using correct containers and labels in line with SOPs and study protocol.
* Instruct study participants on study procedures and use of test materials/devices where appropriate.
* Ensure the study schedule is adhered to and that results are available to other teams on time.
* Maintain records of study activity including CRFs, test material dispensation, and regulatory forms.
* Monitor and maintain clinical stock levels and clerical store levels, ensuring efficient use of resources.
* Prepare data for reporting and study files for archiving.
* Assist with responding to QA audits throughout the life cycle of studies including inspections, data, and reports.
Qualifications
* Awareness of GCP (Good Clinical Practice).
* IT literate.
* Strong attention to detail to identify errors and refine documents for clarity and precision.
* Effective communication skills, both written and oral.
* Organised and able to work in a team or independently.
* Good time management and ability to prioritise.
* Experience in a fast-paced, dynamic environment with shifting deadlines.
* Experience working with cross-functional teams.
Benefits
* Enhanced Annual Leave Entitlement
* Annual Leave Sellback Scheme
* Additional Annual Leave at set service dates
* Free Parking
* Company Pension Plan
* Life Assurance (4x annual salary)
* Healthcare Cash Plan (6+ months service)
* Enhanced Maternity, Adoption and Paternity Schemes
* Employee Assistance Programme 24/7 confidential
* Health and Wellbeing Programmes
* Worldwide career opportunities
What happens next
You'll be invited to meet the team through an assessment centre or staged interview process depending on the role, to see what working for Eurofins is like and to understand your key skills and strengths.
Your data
As part of the recruitment process, the company collects and processes personal data relating to job applicants. The company is transparent about how it collects and uses data and about meeting its data protection obligations.
Closing date
We reserve the right to close or extend this position depending on application numbers. If you apply late, your application may not be considered. If you do not receive a response within 4 weeks of the vacancy expiry date, your application may be unsuccessful.
Equal opportunity and sustainability
We support diversity and are an Equal Opportunity Employer. We prohibit discrimination based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and other characteristics. We encourage sustainable changes and have a carbon-reduction initiative.
Find out more on our career page: https://careers.eurofins.com/
Seniority level: Entry level • Employment type: Full-time • Job function: Science
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