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Clinical Research Associate - Oncology

Prahealth Sciences

United Kingdom

On-site

GBP 60,000 - 80,000

28 days ago

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Job summary

An established industry player is seeking an experienced Clinical Research Associate to enhance their Oncology team. This role offers a unique opportunity to work alongside a renowned global pharmaceutical company, contributing to innovative research in life-saving medicines. You will be empowered in a collaborative environment where your expertise in clinical research monitoring, particularly in Oncology, will be valued. If you are passionate about making a difference and thrive in a dynamic setting, this position is perfect for you.

Qualifications

  • Strong Oncology experience in clinical research monitoring is essential.
  • Candidates must have the right to work in the UK.

Responsibilities

  • Select potential investigators and provide monitoring visit reports.
  • Drive site performance and resolve study-related issues proactively.
  • Train and support investigators and site staff in study matters.

Skills

Oncology experience

Clinical research monitoring

Data query resolution

Performance driving

Job description

Overview

Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team for pharmaceutical and biotechnology company partner.

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory, and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

Responsibilities

  1. Contribute to the selection of potential investigators.
  2. Provide the required monitoring visit reports within required timelines.
  3. Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
  4. Perform source data verification according to SDV plan and ensure data query resolution.
  5. 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.
  6. Train, support and advise Investigators and site staff in study related matters.

Qualifications

We are looking for candidates with strong Oncology experience working in a clinical research monitoring capacity, and residing in Northern England or Midlands, UK (with appropriate right-to-work in the UK already granted, if applicable).

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