This is a full time in-house Medical Writing contract (long term with option to go perm) with a large pharma in the Dallas/Ft Worth, TX area.
Responsibilities:
- Develop, review, and edit technical documents including clinical study protocols, investigator's brochures, study reports, risk assessments, presentations, and regulatory submissions in relation to the safety evaluation of ophthalmic devices
- Perform periodic relevant literature searches and evaluations
Minimum Requirements:
- Bachelor's degree in life sciences
- At least 2 years of medical writing experience in pharmaceutical or medical device industry
Competencies:
- Fluent in English
- Excellent interpersonal, oral, and writing skills
- Detail-oriented and self-motivated
- Fast learner and able to manage changing priorities
- Able to organize, analyze, and interpret data with minimal supervision
- Proficient in MicroSoft Word, Excel, and PowerPoint
Preferred Skills/Qualifications:
- Knowledge of ophthalmology (cataract and refractive surgeries)
- Knowledge of medical device clinical trials and safety reporting requirements
Contact:
Jill Vandergrift jvandergrift@preceptlife.com
Precept Life Sciences
Subsidiary of Cambridge Global Services
727.812.3383 office
800.436.2212 x264 toll free
703.439.2482 fax
www.preceptlife.com
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3 comments:
Great work . Thank you that was very educational, good luck
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Is it Still available.
And will it be applicable if the employee is from India.
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It is great opportunity.
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