Clinical Research Associate, UK

Pharmaceutical Research Associates, Inc; Reading; Remote; GBP 30,000 - 45,000; Full time

Job summary

A global biotechnology company seeks an experienced Clinical Research Associate (CRA) to enhance their UK team. The role focuses on site monitoring, investigator selection, and ensuring data compliance. Candidates should have over 2 years of relevant experience and a right-to-work in the UK. Ideal for those looking to work with a leading organization in the biotechnology field, this position offers the chance to impact the clinical research landscape significantly.

Qualifications

• Minimum 2 years of experience as a UK CRA.
• Residing in the UK with right-to-work.
• Valid driving license.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide monitoring visit reports within timelines.
• Drive performance at study sites and resolve issues.
• Perform source data verification and ensure query resolution.
• Initiate, monitor, and close study sites in compliance.
• Train and advise site staff on study matters.

Skills

Experience as a clinical research monitor

Site performance management

Source data verification

Training and advising site staff

Job description

Overview

Experienced UK-based CRA/clinical research associate required to augment existing CRA team, partnering with a long-standing multinational biopharmaceutical company.

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. The company focuses on a broad range of therapeutic areas and 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 and systems training plan), operating in a large 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/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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