Jr. Medical Writer in Horsham, PA at Integrated Resources, Inc

Date Posted: 5/13/2021

Job Snapshot

Job Description

Client is currently seeking a Jr. Medical Abstract Writer for a long-term engagement with one of our Global Pharmaceutical clients in Horsham, PA.

This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly. This role is full-time and you may be eligible for healthcare and retirement benefits and paid time off.


Manage and/or provide expert, independent writing support for assigned documents and/or publication/therapeutic area team(s). Documents may include but are not limited to abstracts, posters, oral presentations, and manuscripts. May assist with electronic submissions of abstracts, posters, oral presentations, and manuscripts.
Interface with authors on abstracts, posters, oral presentations, and manuscripts.
Manage and/or write, edit, and revise abstracts, posters, oral presentations and/or manuscripts. As agreed upon by the lead author, develop any or all of the following: publication outline, publication shell, draft publication, as well as various other written sections of publications.
Manage and/or review and interpret data and source documents for information required for publication development. Assist in table and figure mock-up development.
Identify and resolve, with the help of other functional areas, clinical and statistical issues in the interpretation of clinical data.
Participate in the development and maintenance of document templates, style guides, electronic document management and publication system, and SOPs.
May perform other duties as assigned.
Provide support and representation to assigned therapeutic area publication team.
Manage document development timelines to facilitate timely submission.
Maintain annotated versions of documents and facilitate review cycles.
Facilitate, collate, and adjudicate author and reviewer comments.
Adjudicate and address quality assurance (QA ) review.
Verify completion of mandatory approvals (eg, Legal, Patents, Regulatory Affairs) prior to manuscript submission.