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Job Details
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Business Type: Pharmaceutical Company, Biotechnology Company, Contract Research Organisation, Drug Development Company
Job Type: Data Management
Job Level: Management
Position: Full Time
Location: USA - Massachusetts
Reference: AC0507
Closing Date: 09/08/18
Job Details:

At the risk of sounding clichéd - there is no other way to phrase it other than this company sets the standards to which all other CROs should strive to meet and they have a demand for Clinical Data Managers with a breath of understanding in managing a study and managing stakeholders expectations.

As a Clinical Data Manager II with this client, your main three objectives will be:

  • Designing eCRF''s and development of Data Validation Plans
  • Assist in the review of Study documents, Development of the data management plan
  • Maintaining healthy relationships with your team and the clients

There will be elements of tracking and reporting of metrics/activities leading to database lock and of course there is an element of training of site staff and project teams on CRF Completion.

This position is for someone who wants long-term stability and is eager to work their way up the ladder by putting in significant ground work from the start.

What they offer:

  • Competitive salary and benefits package
  • Tailored career development to grow aspects of your career you want
  • To work with a well-established group of Data Managers.
  • A stable pipeline of work and plenty of resources to work with.

Your experience should look like this:

  • BSc in a Life Sciences degree
  • At least 4+ years working in a Clinical Trials for a CRO or Pharma
  • Medidata Rave, Oracle InForm, ClinTrial)
  • Ability to work independently and perform multi-task activities
  • Must have the rights to work in the EU region.


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


If you would like to discuss this vacancy further, please call Aoife Cronin on +1347 967 5935, or email If this role is not suitable, Aoife is also available to discuss other possible positions or answer any general questions regarding your career.

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Posted: 12/07/2018 | NPJ Ref: 218276
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