The job Clinical Trial Assistant has been saved.


Ready to apply?

Please confirm your email to start the apply process.
For information about how we process your personal data, see our Privacy Statement.

The Job has been saved succesfully

Enter your email address to save this job

You are saving this job as:

search results

Clinical Trial Assistant posted by Covance Inc.

Full Time

Job Description

Clinical Trial Assistant
Job Location(s) UK-Leeds

Job Number

Job Category
Clinical Operations Entry Level

Position Type

Job Overview

About Covance

Your new employer is Covance Inc., the drug development business of LabCorp®, is the world's most comprehensive drug development company, dedicated to advancing healthcare and delivering Solutions Made Real^®. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow's challenges as they evolve.

Covance are seeking a Research Technician to join the Clinical Pharmacology Team within the European Centre of Excellence in the heart of Leeds, West Yorkshire. You do not need a medical/scientific background for this position, we will provide you with comprehensive training and support.

Key Responsibilities

Your main responsibilities will include but not be restricted to:

* Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings
* Preparation and accurate recording of ECGs/Holters
* Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples
* Monitors meals to ensure dietary compliance by research participants
* Assist in the preparation of rooms and medical equipment
* Assist with screening procedures as needed
* Maintain a clean, safe and efficient working and study environment
* Foster respectful relationships with study participants
* Accurately record all research data obtained or observed
* Assist with QC of source documents and case report forms
* Maintains constant awareness of participant safety and dignity at all times.
* Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.

Education / Qualifications

Skills and Experience Required for this Role

* A good standard of general education


* Previous clinical research experience would be desirable

Reference Number


Similar Jobs