PharPoint Research Inc. attracts the best talent in the industry. Our team members are dedicated to excellence in job performance, thrive in a collaborative environment, and are accustomed to working in a fast paced, dynamic work environment. PharPoint Research is an equal opportunity employer.

Medical Writer

Description: • Write clinical documents for submission to regulatory authorities • Act in the capacity of project manager/lead for medical writing projects. • Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. • Coordinate and conduct interdepartmental team review and sign-off of document deliverables. • Coordinate production and distribution of draft and final documents to project team and client. • Perform literature searches/reviews. • Review statistical analysis plans and mock statistical output to assist in determining appropriateness of content/format for clinical writing. • Provide resourcing estimates for potential new medical writing projects. • Review requests for proposal packages sent by clients to determine content and appropriateness of materials required for development of clinical documents. • Initiate and manage development of formats, templates and general guidelines for clinical documentation and workflow procedures. • In concert with Department Heads, provide technical writing and/or review of template documents, business plans, project proposals, company promotional materials, white papers, blogs, and other forms of written communication.Education: Bachelor’s degree (B.A./B.S.) or equivalent in a Life Sciences/Health Related Sciences or related discipline. Experience: Minimum 3 years of experience in medical writing or related field, preferably in the CRO industry