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Job Details

Senior / Medical Writer, Regulatory (Home-based)-146315

Company: PPD
Location: Europe, Middle East & Africa-SA-Gauteng-Johannesbu
Reference: 146315
Closing Date: 21 Nov 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

As part of our on-going growth, we are currently recruiting for a Senior / Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. ...

Requirements:



As part of our on-going growth, we are currently recruiting for a Senior / Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific.

 
The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist Regulatory Affairs professionals with marketing applications, INDs, paediatric investigational plans, clinical trial applications, and other types of regulatory documents.

 
Our writers possess strong leadership and project management skills, are creative problem solvers and decision makers, are engaging mentors and enthusiastic members of the department with an eagerness to continually improve our offerings and deliver a market leading service to our clients. In return, the medical writing department offers a highly competitive compensation package together with excellent opportunities for personal development and progression within the field. All within a friendly, fast paced and exciting environment.

The Medical Writer collaborates with internal and sponsor team members to interpret, distill, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarisation of preclinical and clinical studies for preparation of investigator's brochures, and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications.


Qualifications


    Education to Bachelor’s/advanced degree level in a scientific discipline
    3 /5 years of experience within regulatory medical writing
    Excellent grammatical, editorial and proofreading skills
    Effective organisational and planning skills
    Motivation, initiative and adaptability
    Ability to work effectively in a team

The successful candidate can look forward to job stability with a leading CRO that has experienced year-on-year growth. We offer a generous salary and benefits package as well as excellent learning and development opportunities. We understand that the best writers are not necessarily on our doorstep, so if you are looking for a home based role we can offer this option to the right candidate, providing everything you need to fulfil your potential from your home office. This position can be home or office based in South Africa.
 
We look forward to receiving your application.

‘Preference will be given to employees from the designated groups in line with the provisions of the Employment Act No.55 or 1998 (and any amendments thereto), PPD’s recruitment policy and the Employment Equity Plan’.

 

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Apply for this job: Senior / Medical Writer, Regulatory (Home-based)-146315

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

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