Clinical Research Associate

4 days left

East Riding of Yorkshire, England
GBP200 - GBP300 per day
Oct 04, 2016
Nov 01, 2016
Bryoni Charles
Result Type
Position Type
Full Time

One of the worlds leading Pharmaceutical Companies are looking for an individual to join their CRA team.....

Title: Clinical Research Associate

Location: Field Based - Regional Monitoring - Yorkshire

Status: 12 month contract

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

Contact: Bryoni Charles

Reference No:

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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