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Job Details

Working for a CRO looking to get into Pharma? Clinical Study Manager - UK / London

Company: Barrington James Clinical
Location:
Reference: ACCTMUKNEWPHARMA
Closing Date: 28 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

This is a great Opportunity for a CTL/CTM to work for one of the most reputable pharmaceutical companies on truly life changing studies that result in saving millions of lives. To find out more message me via acoppen@barringtonjames.com

Requirements:

I’m working on an exciting opportunity for a Clinical Team Manager (CTM/Study Manager) to work dedicated to one of the top, most reputable pharmaceutical companies in the world. You will be working fully integrated to the client’s projects and sites, working within their teams and gaining amazing experience in a pharmaceutical environment.

 

You will be working for a pharmaceutical company that invested over £3Billion into their development of new medicines last year and they recently profiles over 40 potential first-in-class vaccines/medicines in an R&D event which is testament to their great reputation. We have successfully placed a large number of people with this company and the feedback has been phenomenal. The support, training, array of projects, benefits, flexibility are some of the main factors we hear on a regular basis from the employees of this company.

 

The role coordinates all aspects of clinical activities which include:

 

  • Local implementation of international clinical trials and / or local trials entrusted to them, their preparation for their closure, in compliance with GCP, regulatory requirements, SOPs, quality standards, deadlines and budgets
  • Co-ordination of the Clinical Research Associates who are allocated to a project on a Country basis
  • Work in partnership with the project teams to ensure the necessary training, tracking and quality systems are in place for the clinical team
  • Be primarily responsible for the clinical deliverables of the Project within agreed timelines and budget

 

I am looking for individuals with a track record of success on coordinating clinical trials on a CTM/CTL/JPM or Lead CRA level from either a CRO of a Pharma background. This is a great opportunity for those of you working direct for a CRO to gain experience on the Pharma side. You will need to have proficient working knowledge of GCP and experience in several therapeutic area, be comfortable working in a matrix management system and have the ability to motivate, mentor and integrate teams.

 

Education and Experience:

  • Life Science Degree
  • Clinical research experience in all phases of study life cycle, including start up, interim and close out
  • CRO or Pharmaceutical company background
  • Study Coordination experience as CTM/CTL/LCRA ect MINIMUM 12 months – any less will unfortunately not be put forward
  • CRA background

 

This fantastic opportunity WILL be closed by the end of the year due to a number of pivotal projects starting in Q1. We have already successful placed 1 CTM in this company therefore there is a limited number of positions available. To find out more, contact me in the office on 01293776644 or email me via acoppen@barringtonjames.com

Apply for this job: Working for a CRO looking to get into Pharma? Clinical Study Manager - UK / London

Contact Information:

Address:  Head Office
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333

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