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Study Coord I

Covance 4/3/2019 1:56:58 PM
JOB ID: 29692 Category: Clinical Operations Entry Level
Leeds, United Kingdom



Job Overview

Study Coordinator I

* Responsible for logistical set up of study to ensure good study flow and adequate resources are assigned.
* Assists the Clinical Research Coordinator with their responsibilities and acts as their back-up as needed.
* Assists in creation of source documents, labels and study specific instructions.
* Assists in creation of study schedules.
* Orders supplies/equipment and dietary needs for assigned studies.
* Assists in staff training of study specific procedures.
* Coordinates tasks related to participant check in and discharge and may assist with resolution of participant issues.
* Is present in the clinical work areas for critical events or as assigned by a senior team member.
* Completes sample shipment documentation as necessary.
* Compiles data tables/summaries as requested.
* Assists with the compilation of protocol and SOP deviations.
* Attends all required meetings as appropriate.
* Maintains skills to perform study tasks and assists with study procedures as necessary.
* Maintains accurate records of all work undertaken.
* Maintains an understanding of FDA, GCP and ICH requirements.
* Maintains constant awareness of participant safety and dignity at all times.
* Ensures that client and participant confidentiality is maintained.
* Responds to team queries in a timely manner.
* Takes ownership for the quality and standard of own work.
* Performs other related duties as assigned.

Education / Qualifications

* University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
* In lieu of a degree, typically 1 years Experience in related field (e.g. pharmaceutical, laboratory, data analysis) will be considered in addition to the Experience requirement.


* Typically 6-12 months of professional work Experience . Experience in clinical research is preferred.
* Basic knowledge of computer and programs (e.g. Microsoft Word, Excel).
* Knowledge of drug development process, ICH Guidelines and GCP.

Position Type: Full-Time

Location: Leeds, UK - United Kingdom


Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).