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Clinical Study Management Associate - Biotech - 12m Contract



Business Type: Pharmaceutical Company, Biotechnology Company, Drug Development Company, Freelancer, Pharmaceutical Services
Job Type: Clinical Research Associate (CRA), Clinical Operations, Clinical Study- Trials, Senior Clinical Research Associate (SCRA), Project Management
Job Level: Experienced (non manager)
Position: Contract
Location: London
Reference: 040619LMCQ1
Closing Date: 30/08/19
Job Details:

Clinical Study Management Associate - Biotech - 12 Month Contract

i-Pharm Consulting are seeking on behalf of a major Biotech a Clinical Study Management Associate to support the management of outsourced studies across a range of EU countries. This role will see you supporting Liver Disease studies. This contract is perfect for a CRA with recent 6-12 months Study Management Associate level experience looking to step into Project Management.

THE COMPANY

Leading Biotech with a global presence in over 100 countries. i-Pharm has been a dedicated recruiter for this client for a number of years and have had great feedback on the company''s career progression, culture and job satisfaction from candidates placed in both permanent and contract positions.

TITLE:

Clinical Study Management Associate

THE ROLE:

You will be involved in:

  • Supporting management of EU outsourced studies
  • Provide administrative support in site selection and coordination of studies
  • Assist Clinical Trial Managers with vendor and CRO management
  • Co-monitor approx. once every 2 months across a number of EU countries
  • Under supervision of the CTM assist in review of ICFs, CRFs, SOPs, monitoring plans and study reports
  • Support training of Clinical Project Assistants and Clinical Trial Management Associates
  • Support the set up and presenting of investigator meetings

EXPERIENCE:

  • Life Science degree
  • Ability to travel 20%
  • Experience in liver disease is preferred but not essential
  • Some Assistant Project Management or Trial Management experience is preferred but not essential
  • MUST HAVE independent monitoring CRA background
  • Good knowledge of ICH-GCP Guidelines

LOCATION:

Office Based - West London

2 days work from home flexibility

DURATION:

12 Month Contract - Freelance

RATE:

£350 per day

ABOUT i-PHARM CONSULTING:

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

TO APPLY:

If you would like to discuss this vacancy further, please call Lauren McQuade on +44(0)2031890488, or email lmcquade@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEYWORDS:

Associate Study Manager / CTMA / Clinical Trial Manager / Trial Management / Trial Management Associate / Study Manager / Associate Project Manager / Study Management / Biotech / Biotechnology / Biopharma / Biopharmaceutical / Pharmaceutical / CRO / Clinical Research Organisation / Inflammation / Liver Disease / GI / Infectious Diseases / HIV / Phase IV / Late Phase / London / West London / Uxbridge / Hayes / Buckinghamshire / Maidenhead / High Wycombe / Marlow / Slough / Reading



i-Pharm Consulting Posted by:: i-Pharm Consulting (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 23/08/2019 | NPJ Ref: 240728
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