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Job Details

Medical Writer 2 - Office based Livingston UK

Company: Quintiles
Location: Livingston
Reference: 1623974
Closing Date: 19 Feb 17
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

Are you a regulatory medical writer, who thrives on a busy and varied workload in a global working environment? Demand for Medical Writing services from QuintilesIMS continues to grow!  We are looking for new colleagues to join our enthusiastic, loyal and friendly team and help us to help our customers get new medicines to patients. ...

Requirements:

Are you a regulatory medical writer, who thrives on a busy and varied workload in a global working environment?
 
Demand for Medical Writing services from QuintilesIMS continues to grow!  We are looking for new colleagues to join our enthusiastic, loyal and friendly team and help us to help our customers get new medicines to patients.  If you are looking for a new challenge, a wide variety of therapeutic and product experience, an international working environment with a strong future, and an employer that cares about its staff and values a good work-life balance, QuintilesIMS could be the company for you. 
 
To meet our needs, the successful applicant will have:

  • experience in working as part of a team on protocol and CSR projects in Phase II and III. Candidates with strong experience in Phase I/IIa trials may also be considered.
  • the ability to communicate confidently, assertively, and diplomatically, both verbally and in writing, with international project teams.
  • a solid scientific academic background, together with existing regulatory medical writing experience and an understanding of clinical drug development.
 
Depending on level of experience, the successful applicant should also be able to:
  • understand and interpret study objectives and clinical trial data and the regulatory and scientific requirements of the documents we prepare.
  • confidently work with others to develop study protocols from brief outlines, and take responsibility for a variety of clinical documents for a wide range of both international and local sponsors, across all therapeutic areas.
  • interact directly with international project team members and sponsors, proactively manage his/her own deliverables, and identify and respond appropriately with solutions to any potential issues and problems.
  • multi-task, balancing project lead roles with review responsibilities for others, and helping out colleagues in the team on a planned or ad hoc basis.
  • work with minimal direction on most assignments, identify project needs, and create project timelines.
  • review the work of others and provide appropriate feedback.
 

To meet our needs, the successful applicant will have:
  • experience in working as part of a team on protocol and CSR projects in Phase II and III. Candidates with strong experience in Phase I/IIa trials may also be considered.
  • the ability to communicate confidently, assertively, and diplomatically, both verbally and in writing, with international project teams.
  • a solid scientific academic background, together with existing regulatory medical writing experience and an understanding of clinical drug development.

Apply for this job: Medical Writer 2 - Office based Livingston UK

Contact Information:

Address:  .
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England
Website:  Visit Our Web Site

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