Clinical Research Technician

Employer
Covance
Location
Leeds, , United Kingdom
Salary
Competitive
Closing date
2 Oct 2020

View more

Discipline
Clinical Research, Clinical Operations
Hours
Part Time
Contract Type
Permanent
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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 Clinical Research Technician to join the Clinical Pharmacology Team within the European Centre of Excellence in the heart of Leeds, West Yorkshire in a bank position. You do not need a medical/scientific background for this position, we will provide you with comprehensive training and support . You will need a flexible approach to working as this position will include day/evening/weekend shifts.

Key Responsibilities

Your primary responsibility will be to take biological samples from staff and healthy volunteers as part of Covance's COVID-19 testing programme, completingthe required paperwork and preparing test samples for shipment.

Your responsibilities may 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:
  • A good standard of general education,particularly in science subjects.
Experience:
  • Previous clinical research experience would be advantageous.

Covance Profile Page image

Join our growing team and discover your extraordinary potential


We are recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, our comprehensive service portfolio provides the opportunity to explore diverse projects and unique career paths across the drug development spectrum.

Please visit our Careers Hub

Learn more about our work to improve health and improve lives:

https://youtu.be/Wx2wxyLd7no

Contact Us
  • Maidenhead Office Park
  • Westacott Way
  • Maidenhead
  • SL6 3QH
  • United Kingdom
  • Mini-site: Covance
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