Clinical Screening Technician

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

View more

Discipline
Clinical Research, Clinical Operations
Hours
Part Time
Contract Type
Permanent
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Job Overview:

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. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner. Excellent opportunity for a ScreeningTechnician to join our Phase I Clinical Research business in Leeds, West Yorkshire in a bank position. This is a great opportunity to begin your career within Clinical research/trials and allow you to continue to practice your clinical skills and knowledge inearly phase clinical trial studies.

Key Responsibilities

Your main responsibilities will include, but not be restricted to:
  • Read protocols in order to assist with screening procedures necessary to determine participant qualification as well as to understand the Inclusion and Exclusion criteria for the study.
  • Work with Project/Study Manager and Screening/Recruitment Supervisor to arrange any special screening procedures that may be necessary for the study.
  • Provide assistance to ensure that recruiting questionnaire is accurate in helping to determine eligibility of study participants.
  • Assist with the preparation and organization of all necessary materials for participant screening and physical exams including, medical history packets, Informed Consent packets, participant calendars and any other necessary documents and/or forms required for the study.
  • Obtain informed consent and medical history from screening volunteers
  • Ensure that all necessary screening tasks have been performed including height, weight, frame size, venipuncture, vital signs, electrocardiograms, spirometry and simple laboratory procedures as needed and required per the study protocol.
  • Review screening charts for accuracy and completeness.
  • Prepare screening charts for Project/Study Manager and Physician review.
  • Maintain the status of study subjects in the database.
Education/Qualifications:
  • Educated to GCSE Standard or equivalent.
Experience:
  • Previous clinical research experience may be substituted for education requirements.

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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