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Medical Writer

PSGGlobalSolutions2

Chesterfield, MO, United States contract

Posted: June 15, 2016

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Quick Summary

We are seeking a Medical Writer to join our team in Chesterfield, MO, where we deliver exceptional service levels, change the lives of our clients, and partner with top pharmaceutical, biotechnology, and medical companies.

Job Description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:

• Assist with verification of data within regulatory documents or reports.
• Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.
• Create drafts of new technical or regulatory documents using existing examples, templates or reports
• Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.

SKILLS:

• Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
• Regulatory, GMP or Pharmaceutical experience, preferrably in bioprocess or cell line development areas is desirable
• Detail oriented

EXPERIENCE:

• 3-5 years

EDUCATION:

• Scientific Background; BS or higher Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP!

I want to know more about your preferences. If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!

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