Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials in line with ICH-GCP and sponsor requirements. You will ensure site initiation, monitoring visits, safety reporting, and study materials coordination, with a strong focus on regulatory compliance and timely issue resolution.
The role demands at least 8 years in CRA roles, a bachelor-level science degree, and proven MS Office skills.
#J-18808-Ljbffr
Full job description from WhatJobs. Apply for this role →
Normanton on Trent
Tigermed is seeking a seasoned Clinical Research Associate in the United Kingdom to oversee site management, training, and documentation across…
West of England
Tigermed is seeking an experienced Clinical Research Associate to lead site management for UK trials.
Wollaton
Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across…
Berkshire
In this role you lead Local Study Teams at country level to deliver study commitments on time and with quality, aligning with Sponsor procedures and…
Remote
You will support and oversee clinical studies from a home-based role in the UK or Northern Ireland, ensuring studies are conducted to protocol…
Langley
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory…
Explore: Site Manager jobs in Manchester Site Manager jobs in the UK Specialist jobs in Manchester
Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.