Study Assistant

Frontage Laboratories•Concord, OH

4d•Onsite

About The Position

We are seeking a highly-motivated, detail-oriented team member to support client-driven projects. The successful candidate will be an active member of the Study Support Group and will assist Study Directors on assigned studies with general client needs, drafting and issuing protocols/protocol amendments, preparing subreports, running Provantis data tables, and reviewing study data all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines.

Requirements

Associate’s or Bachelor’s Degree preferably in Life Sciences, communication, English, or similar related discipline.
An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education.
Willing to train individuals with correlating background, education, or skills.
Proven ability to successfully work in a team environment.
Excellent oral and written communication skills.
Basic computer knowledge (e.g. Microsoft Word, Excel, Adobe Acrobat)

Nice To Haves

Experience with Provantis or similar LIMS software is a plus.

Responsibilities

Generate Provantis data tables and create PDFs of tables for reporting
Draft subreports (Ophthalmology, Anatomic Pathology, Clinical Pathology, ECG), protocols, and protocol amendments.
Review study data, data binders, and documents generated by Study Directors/Study Support as needed.
Assist with drafting deviations as they arise
Update Toxicology Project Management system as milestone tasks are completed.
Review and edit grammar, styles, typefaces, and formatting based on report writing style guidelines for all generated documents.
Reviewing Locomotor Activity Data spreadsheets and ECGs.
Data entry into Provantis for various studies