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Medical Writer

Bangalore
Permanent
Reference: JR066811
Description

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them?

At ICON, we have an incredible opportunity for outstanding Medical Writers across different levels (Narratives: 3 to 14 years of experience) to join our team in Bangalore office. This is a rare opportunity to join our friendly global Medical Writing team which sits within ICON's Clinical Research Services group. Our remit is to produce high quality documents supporting clinical studies and regulatory submissions.

The Role

  • Write the reports of clinical trials and other regulatory documents (including patient narratives for serious adverse events and drop-outs due to non-serious adverse events) according to ICON or client-specified formats

  • Provide additional writing and editing services (e.g. for publications) as required

  • Assist in the production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews, and other documents needed for regulatory submissions

  • Assist in quality control (review) of documents

  • Liaise with internal groups, i.e. Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical and Quality Assurance to obtain the necessary information and to ensure the timely implementation of activities related to the production of reports

  • Write narratives independently, lead narrative projects and mentor junior writers as required (depending on seniority of the role considered for)

  • Ability to write multiple document kinds, handle projects independently with minimal supervision, efficiently manage client needs and expectations

What you need

  • Bachelor's degree in a life science/health related sciences, or equivalent

  • Medical/Technical writing experience of 3 to 14 years in a clinical research setting

  • Ability to assimilate and summarize large volumes of scientific data accurately, clearly and concisely

  • Strong written and oral communications skills

  • Strong word processing skills including familiarity with MS Office products for documentation and presentation development

  • Understanding of clinical research, the drug development process, and applicable regulatory guidelines

Why join us?

Ongoing development is vital to us, and as a Medical Writer, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international and we sincerely care about our people and their success.

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