Site Activation Coordinator - Reading, United Kingdom - IQVIA

IQVIA

Verified Company

Reading, United Kingdom

3 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Job Overview

Perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.

May also include maintenance activities.

Essential Functions

Perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions
Prepare site regulatory documents, reviewing for completeness and accuracy.
Inform team members of completion of regulatory and contractual documents for individual sites.
Distribute completed documents to sites and internal project team members.
Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications

Bachelor's Degree Life sciences or a related field.
1 years' experience in a healthcare environment or equivalent combination of education, training and experience.
General awareness clinical trial environment and drug development process.
Ability to work on multiple projects.