Clinical Research Associate - Oncology

Prahealth Sciences; United Kingdom; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking an experienced CRA/Clinical Research Associate to join their Oncology team in the UK. This role involves site management, performance driving, and supporting clinical studies within a collaborative and innovative environment aimed at enhancing patient care. Candidates should possess strong Oncology experience and be located in Northern England or the Midlands.

Qualifications

• Strong Oncology experience working in clinical research monitoring.
• Residing in Northern England or Midlands.
• Right-to-work in the UK already granted.

Responsibilities

• Contribute to the selection of potential investigators.
• Drive performance at the sites and identify issues.
• Train and support investigators and site staff.

Skills

Oncology experience

Clinical research monitoring

Problem-solving

Job description

Overview

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

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

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)

#LI-Remote

#LI-DB1