Clinical Research Associate, UK

ICON; United Kingdom; Remote; GBP 30,000 - 45,000; Full time

Job summary

ICON, a leading independent biotechnology company, is seeking an experienced Regional Clinical Research Associate (CRA) to join their UK team. This rewarding position involves monitoring site activities and improving performance to ensure compliance with study protocols. With strong support and training opportunities, the role offers a chance to contribute significantly to projects aimed at addressing unmet medical needs in society.

Qualifications

• Strong experience (~>2 years') as a CRA.
• Driving License.
• Right-to-work in the UK.

Responsibilities

• Contribute to investigator selection.
• Provide monitoring visit reports timely.
• Initiate, monitor and close study sites.

Skills

Monitoring

Performance Improvement

Data Verification

Training

Job description

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).

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.

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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