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Job Details

Associate Director, Clinical Research

Company: RBW Consulting
Location: Wales
Reference: RNBWMMCA
Closing Date: 01 Sep 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent package as part of the Medical Operations team.

Job Summary:

A world-leading Research Organisation that is currently undergoing expansion is seeking a new Associate Director who shares their ideals of patient safety and delivery of high standards of clinical research to join their site in Wales.


Associate Director, Clinical Research. Wales

Advertised by Ryan Worth at RBW Consulting


As Associate Director, you will be responsible for the overall performance and safety of the research sector as well as line management of the clinical research physicians on-site.

You will also take on the role of Principal Investigator alongside your site management duties; managing the studies and patients whilst ensuring ICH/GCP and local regulations are met.


Operations Manager Duties:

  • Reviewing screening, pre-screen and screen success rates for clinical trials and cooperate with CM and UK Senior Research Physicians to ensure and optimise delivery.
  • Ensure implementation of Core Competency framework at the site level and work within the medical management matrix in order to support the training and development of the medical team.
  • Support the Centre Manager in the delivery of safe clinical trials with a focus on supporting the optimisation of the Profit and Loss of the centre with regards to recruitment revenues against projections.
  • Assist in reviewing SOPs and provide appropriate feedback and suggestions for improvement.
  • Demonstrate leadership through the guidance and training of colleagues while working on multiple studies or multiple sites.
  • Liaising with and developing positive relations with sponsors, clients and clients’ contractors as required, projecting a helpful and courteous company image

Principle Investigator duties:

  • Conducting clinical trials in line with the protocol and to ensure the recruitment of eligible participants onto the study
  • Taking responsibility for the medical wellbeing of participants during the clinical trial and referral to specialists or GP as required
  • Taking responsibility for ensuring serious adverse events / adverse events are reported appropriately
  • Participate in internal audits where required
  • Mentoring all Research Physicians
  • Ensure quality and delivery at site level by cooperating with the Centre Manager, UK Operations Manager and Senior Research Physician


  • Be a GMC registered doctor with a number of years of previous experience within clinical research
  • Have extensive research experience demonstrating expertise in clinical research
  • Work experience as principal investigator
  • Have working knowledge of GCP (ICH-GCP and local regulations compliance)
  • Demonstrate leadership skills
  • Exercise meticulous attention to detail in recording patient information and data ensuring any queries are acted upon in a timely and efficient manner
  • Communicate all decisions and actions with your colleagues, demonstrating a helpful and flexible approach

How to Apply

If you would like to apply, then please get in contact on;

01293 584300


Apply for this job: Associate Director, Clinical Research

Contact Information:

Address:  Head Office
Origin Two 106 High Street, Crawley RH10 1BF
RH10 1BF
Tel:  01293 584 300
Fax:  01293 534 133
Website:  Visit Our Web Site

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