CRA - Regional Monitoring - Midlands


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Job ID :


Company Type :

Staffing Firms

Industry :


Education Level :


Address 1 :

United Kingdom,West Midlands,West Midlands,

Key Skills :

CRA, clinical research associate, monitoring, monitor, regional, ich, pharmaceutical, midlands

Salary :

£280 - £310 per day

Date Posted :

24 May, 2016

Company Name :


Location1 :

West Midlands

Job Category :

Clinical Monitoring Jobs

Experience :


Job Type:


Travel Amount:

upto 75%


Clinical Research Associate

Field Based - Regional Monitoring - Midlands

12 month contract

Daily Rate: c£300 per day (Ltd Company)

Contact: Alex Butcher

Reference No: 224836

Role Purpose

To manage allocated study sites to ensure that timelines, recruitment and quality standards are met on all clinical trial projects.

Area of Accountability


Manage study sites to ensure investigators fulfil study contracts with respect to recruitment and data quality.

Maintain awareness of ICH GCP, SOPs and regulatory requirements and ensure adherence by site staff

Foster good relationships with investigators, site staff and key opinion leaders



Communicate effectively both verbally and in writing with investigators, other site staff and members of the Clinical Research and Medical Departments in relation to the conduct and progress of clinical trials and resolution of issues.

Proactively participate in investigator or team meetings as required

Problem Solving & Innovation


Identify repeat problems and suggest solutions

Resolve site non-compliance and data quality issues ( protocol violations, ICH GCP, SOPs) and feedback to Clinical Monitor.



Provide clear guidelines and share information with investigators on study objectives and procedures to build their understanding of expectations and targets.

Role Dimensions


Manage 10-20 sites across a variety of projects and therapeutic areas

Role Specific Knowledge, Skills and Experience at Entry


Graduate Life Science/Nursing or Nursing qualification (RGN or equivalent)

Working knowledge of ICH GCP and clinical trial methodology

12 months monitoring experience

Therapeutic Areas: Oncology or Radiology

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