milibicycle.blogg.se - Medical writer jobs florida

#MEDICAL WRITER JOBS FLORIDA SOFTWARE#

The work will include meeting with subject matter experts, conducting research on products and technology, and understanding processes to produce documentation that is easy to understand, branded, accessible, and using the templates and processes for OIT's Knowledge Management procedures.Īssist with editing and updating knowledge articles in the Self-Service Knowledge Base (100+ articles). The position will be writing various documents (standard operating procedures, how-to instructions, user guides, etc. Strong communication skills, both written and oral, with experience in writing standard operating procedures, user guides, etc.Įxperience and expertise in creating accessible documents in Google Suite (using appropriate formatting, co-authoring, etc.).Įxperience documenting information in a clear and logical format to present information for greatest reader comprehension.Įxperience producing written work regarding computers or information technology for an audience of members of the general public preferred. : Denver, Colorado - This can be 100 percent REMOTE! Candidates must be located in Colorado Detail oriented and meticulous follow through.Communicate effectively in English, both oral and written.

Proficient in Microsoft Office (Word, Excel, and Power Point) and Smartsheet.

Knowledge of cGMP requirements for pharma / biotech industry.

Knowledgeable about ICMJE (International Committee of Medical Journal Editors) and GPP3įUNCTIONAL / TECHNICAL KNOWLEDGE & SKILLS:.

#MEDICAL WRITER JOBS FLORIDA SOFTWARE#

Proficient in word processing and pertinent software (e.g., Microsoft Office, EndNote).Ability to lead and/or facilitate effective team meetings for deliverables.Ability to apply project management skills to advance numerous projects at a time and to deliver high-quality documents rapidly.Exceptional analytical, communication, organizational, and interpersonal skills.Experience collaborating with clinical investigator authors/collaborators on documents and publication development.Experience working in a matrix team setting.Experience preparing clinical research documents, and manuscripts for publication in peer-reviewed medical journals as well as abstracts and posters or oral presentations for scientific congresses.PhD, MD, or PharmD with at least 3-5 years of clinical documentation and publication development experience for industry in the bio-pharmaceutical sector.Minimum 5+ years of direct scientific writing experience or 3+ years' experience with advanced degree.Advance degree strongly preferred (MS, PhD, MD, PharmD, etc.). Minimum Bachelor's Degree in a scientific field of study.Maybe responsible for training, mentoring or supervising junior staff members.Management of CRO medical writing relationship with regard to all protocol documents, FDA filings, and site communications like memos or addendums.Establish, maintain, and expand business relationships with cross-functional team members collaborating on publication projects to ensure accurate and timely completion/delivery of information based on publication plans.Draft and edit abstracts, posters, and slide decks for presentation at scientific and medical congresses.Ensure quality, alignment with objectives, and timely completion of publications while staying on track with allocated budgets.

Drive documentation project timelines and handle multiple projects at a time may support one or more products.

Support documents and publication strategies and prioritization of documents and publications.

Understand the publication landscape (e.g., journals, congresses, readership) and advise key stakeholders accordingly.

Maintain relationships with internal and external collaborators/authors on assigned documents and supports process improvement.

Understand and use product strategy, communication objectives, and lexicon appropriately to ensure alignment with publication content.

Appropriately communicates the scientific significance and value of all documents to the target audience, consistent with business processes and compliance requirements.

Manage multiple documents across different molecules/projects and obtain feedback from all key partners to define and implement documents strategies.

Performs Quality Control checking and proof reading of all required documents to meet customer expectation.

Generate content in collaboration with authors/collaborators for protocols, investigator's brochure, clinical study reports, safety updates, abstracts, posters, orals, manuscripts, and slide sets working from various data sources.

This is a hands-on position that primarily includes writing and critically editing scientific manuscripts, abstracts, and podium presentations.

The Medical Writer role will collaborate with internal and external key team partners to develop clinical documents, abstract and publications that are aligned with the Company objectives.