Hobson Prior is working with a small CRO on an exciting Director of Clinical Operations job. The role is based in Hertfordshire and will give you the chance to provide senior oversight to all operational aspects for implementation of clinical trial activity.
Director of Clinical Operations Hertfordshire
Liaise with various internal team members and external stakeholders to ensure the timely, high quality and profitable delivery of projects
Monitor clinical site performance metrics, reviewing regulatory submissions, patient recruitment and progress to study deliverables and timelines
To ensure compliance with required regulatory and GCP quality standards and consistency with Bioclinical-Emas SOPs by offering oversight to Trial Master File (TMF) and TMF Administrators for projects
Cross-reference study budgets with contracted activities for allocated projects, providing monthly draft client invoices and identifying any out of scope activities
Act as global project lead or project lead as assigned and monitor studies to make sure they are performed and conducted in compliance with ICH-
GCP guidelines, SOPs, the protocol and study plans and all relevant regulatory requirements
Can work efficiently across departments and with various external vendors across miscellaneous communication platforms
Ability to coach and mentor project managers, CRAs, system managers and CTAs
Can proactively identify issues and troubleshoot applying problem-solving experience as required
Perseveres and stays extremely motivated and proactive when faces multiple tasks and deadlines
Proficient in the use of Microsoft Office, creating and formatting documents and ensuring consistency across all work
Science graduate (or appropriate level of experience as a healthcare professional)
Minimum of 5 years’ experience in study project management and prior management of contracted resources and vendors
Experience as a line manager is essential
A higher degree or project management qualification would be advantageous
Apply now :
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