Pharsight® Employment Opportunities
Medical Writer
- Business Unit: Pharsight Consulting Services (PCS)
- Reports to: Senior Director, Operations
- Location: Montreal, Canada
Job Responsibilities:
- Critically assess and interpret investigational and medical data and, in that context, accurately write the safety portions of clinical study reports
- Review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation
- Create and/or review a wide range of medical and scientific documentation in support of regulatory submissions (e.g. statistical analysis plans, interim safety and pharmacokinetic reports for ascending dose studies, clinical study reports, executive summaries, integrated summaries of efficacy and safety, and case report forms)
- Create patient narratives in multiple therapeutic areas
- Assist in the writing and review of study reports, conference abstracts, and manuscripts
- Ensure that work is delivered on time and within budget in order to achieve business results for PCS.
Education, Training and Expertise:
Any combination of education and experience providing the required skills and knowledge for successful performance will be considered. Typical qualifications would include:
- Bachelor's, Master's, or PhD (or equivalent) in a specialtyarea such as pharmaceutical sciences, pharmacology, biology, biochemistry or a related discipline
- Minimum two years of experience in medical writing with a focus on preparation of clinical study reports for regulatory submission
Skills and Abilities:
- Excellent verbal and written communication skills in English
- Good general knowledge of drug development process and a demonstrated knowledge of pharmacokinetics and pharmacology
- Works well independently as well as part of a team
Special Requirements:
- Percentage of travel: < 10%
Email resume to: hr@pharsight.com
OR Send to:
Attn: Human Resources
Pharsight - A Certara Company
1699 South Hanley Road
St. Louis, MO 63144
NO PHONE CALLS OR THIRD-PARTY AGENTS PLEASE.