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Clinical Research Associate - Oncology

Symphony Health

United Kingdom

On-site

GBP 60,000 - 80,000

30+ days ago

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Job summary

An innovative pharmaceutical partner is seeking an experienced Clinical Research Associate to enhance their Oncology team. This role offers the chance to work closely with a renowned global pharmaceutical company, contributing to life-saving research in a supportive and empowering environment. If you have a strong background in Oncology and clinical research monitoring, this position provides an opportunity to make a meaningful impact while collaborating with dedicated professionals. Join a team where your expertise will be valued, and help drive the success of critical studies that improve patient outcomes.

Qualifications

  • Strong Oncology experience in clinical research monitoring is essential.
  • Candidates must reside in Northern England or Midlands, UK.

Responsibilities

  • Contribute to investigator selection and provide monitoring visit reports.
  • Drive site performance and resolve study-related issues proactively.

Skills

Oncology experience

Clinical research monitoring

Data verification

Study site management

Education

Degree in Life Sciences

Clinical research certification

Job description

Overview

Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team for a 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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