Clinical Research Associate, UK

Symphony Health; Reading; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology company seeks an experienced Regional CRA in the UK to support study monitoring and investigator training. This position involves contributing to site performance and managing data verification tasks, along with receiving robust internal support. It offers a unique opportunity to impact healthcare positively.

Qualifications

• Strong experience (~>2 years') working as a UK clinical research monitor.
• Currently residing within the UK with appropriate right-to-work.
• Valid Driving License.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide required monitoring visit reports within timelines.
• Drive performance at study sites and identify issues.

Skills

Monitoring site performance

Data query resolution

Training and advising site staff

Job description

Overview

Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for multinational biopharmaceutical company partner.

You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

This is a rewarding and interesting position with a key Global client, with a strong internal support structure in place (including a mentoring training plan) in a big team of ICON staff.

For this role - there is a requirement for 1x internal interview only (and immediate feedback).

Responsibilities

Amongst other tasks, your main responsibilities will be to;

• Contribute to the selection of potential investigators.
• Provide the required monitoring visit reports within required timelines
• Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
• Perform source data verification according to SDV plan and ensure data query resolution
• Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
• Train, support and advise Investigators and site staff in study related matters.

Qualifications

Strong experience (~>2 years') working as a UK clinical research monitor (or CRA), and already residing within the UK (with appropriate right-to-work in the UK already granted, if applicable)

Driving License.

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