Clinical Research Associate, UK

Prahealth Sciences; Reading; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading biopharmaceutical company in Reading is seeking an experienced Clinical Research Associate to join its team. You will be responsible for conducting monitoring activities, training site staff, and ensuring compliance with study protocols. Candidates must have over 2 years of clinical research experience in the UK and a valid driving license. This role offers a supportive environment with a focus on performance management and investigator selection.

Qualifications

• Strong experience (>=2 years) as a UK clinical research monitor/CRA.
• Residing within the UK with appropriate right-to-work.
• Valid driving license.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide monitoring visit reports within timelines.
• Drive performance at the sites and identify study-related issues.
• Perform source data verification and resolve data queries.
• Initiate, monitor, and close study sites per client documents.
• Train and support Investigators and site staff.

Skills

Clinical research monitoring

Source data verification

Performance management

Investigator training

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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