Revel IT
Published
September 14, 2020
Location
Tucson, AZ
Job Type
Work Setting
In-office

Description

OUR GOAL:
Treat our consultants and clients the way we would like others to treat us — we are honest, stay true to our word, and work in the best interest of our clients, consultants, and candidates. Many say they work this way, but few actually do. We are a company that does. Additionally, we bring joy to the world of IT staffing and IT recruiting by making the hiring experience memorable, fun, and different. 

OUR MISSION:
Find and provide the best talent for clients and excellent career opportunities for consultants and candidates — whom we treat as part of our team. Interested in joining our team? Check out the opportunity below and apply today!

Reference:  419321

We are in search of a Medical Writer for a contract role supporting all medical writing activities associated with the Clinical Affairs group with our client. You must be able to work independently with project team members and the Biostatistics and Data Management staff to draft, edit, and finalize a variety of documents including study protocols, presentations, manuscripts for peer-reviewed publications, clinical study reports and submissions to the Food and Drug Administration (FDA).

ESSENTIAL FUNCTIONS:

Designs scientifically sound studies in conjunction with project teams in Biostatistics and Data Management to support new product development in molecular probes, immunohistochemical reagents and new instrument platforms.
Drafts clinical study protocols and study reports. Provides editorial assistance in support of scientific publications and/or post-marketing study activities.
Interfaces with Regulatory Affairs and other groups within the client to ensure the accuracy and timely review and revision of all cross-functional documents supporting regulatory submissions.
Develops scientific expertise in the application of new diagnostic reagents to personalized healthcare.
Educates members of the Clinical Affairs staff in the area of effective visual and written communication; ensures content contained in all documentation conforms to company design control and legal requirements.
Supports one or more clinical development programs.
Ensures high quality documentation with regard to scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines.
Maintains quality system documents pertaining to the clinical affairs group.
Monitors work to ensure quality, and continuously promote Quality First Time.
May perform other duties as required or assigned.

QUALIFICATIONS:

Bachelor of Science, with graduate coursework in molecular biology/cell biology/biochemistry or in a related field (completed AMWA, CMPP, or CMWP certification is desired as well).
Two years of experience in protocol development, data analysis and report writing in clinical or non-clinical studies.
Experience in study design and data analysis.
Expert knowledge and application of scientific principles and concepts.
Demonstrated proficiency in typing, use of Adobe Acrobat 9 Pro and Microsoft Office 2010 products including Microsoft Word, Outlook, and PowerPoint.
Experience with EndNote X2.0 and Microsoft Visio 2010 preferred.
Excellent and proven leadership skills, team skills, written and oral communication skills.
Strong ability to handle multiple projects simultaneously.
Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.
Advanced technical writing skills.
Ability to produce reports and documents independently and evaluate the writing of others.
Demonstrated creativity and ingenuity through the development of novel, multi-disciplinary approaches to projects and strategic issues.
Skill and ability in implementing strategic projects, acting as a catalyst to remove organizational barriers, reduce cycle times and direct process improvements.
Ability to rapidly develop expertise in FDA guidelines for in vitro diagnostic devices and the statistical basis for sensitivity, specificity and reproducibility testing required for validation and FDA clearance and approval.
Ability to rapidly develop expertise in the company’s internal document management system.
Manager’s Must Haves:
Sound logic and reasoning.
Solid understanding of the scientific method and how to design an experiment.
Ability to write clearly and concisely.
Proficient keyboarding.
Interacts well with others.
Capable of working independently.

PREFERRED:

Experience in regulatory writing is preferred.
Experience in design control processes is preferred.
Experience with approval of in vitro diagnostic devices is preferred.
Oncology experience is preferred.

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