Freelance Freelance Medical Proofreader
Job Description
Brella Productions, a new-media production company, is seeking a freelance Medical Proofreader to start immediately.
There is currently a temporary opening for an experienced Freelance Medical Proofreader to join our team on-site at a client’s suburban North Chicago, IL location (near Gurnee, IL). The medical proofreader’s role will be to proof high quality educational & marketing materials that communicate information about the client’s research and products to both medical and consumer audiences. The proofer must be skilled in medical writing, proofreading, research, referencing/annotating, and have American Medical Association Styleguide expertise.
Job Description
Execute medical proofreading and writing activities for projects in accordance with applicable U.S. and international regulatory regulations and requirements under the supervision of the Agency Manager.
Assume primary responsibility for proofreading of regulatory response documents and documents supporting major regulatory submissions, under the direction of the manager.
Proofread documents for submission to FDA or other regulatory agencies, in accordance with team input, with oversight from the manager.
Provide review and substantive editing of contributions from external contract writers.
Skills
Extremely detail oriented
Exceptional organizational skills
Exceptional writing skills
Exceptional proofreading skills
Must be highly proficient in Microsoft office products
Able to set and maintain both short and long term deadlines
Able to take notes, self manage and follow through on complex projects
Able to troubleshoot difficult or sensitive problems and find positive solutions
Qualifications
Bachelor’s degree in science, health profession, or journalism.
Minimum of 2-3 years experience writing for pharmaceutical, biotechnology or equivalent experience (e.g. academia or scientific publications).
Advanced degree in science, health profession, or journalism is preferred.
Basic understanding of scientific methodology, with ability to understand clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission.
Able to understand FDA/international regulations, ICH guidelines, and applicable U.S./international regulatory processes related to document preparation and production (including CTDs).
Able to understand guidelines and requirements related to the preparation and production of regulatory documents and submissions.
Demonstrate problem-solving and interpersonal skills that facilitate effective interactions within cross-functional teams and with external providers.
Able to identify issues and generate solutions or request appropriate intervention by management.
Able to drive to or commute via Metra to the client site in North Chicago.
How to Apply
Interested parties should submit all resumes and references to jobs@brella.com
No phone calls please.
No Recruiters please.
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