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. Molina Healthcare is an Equal Opportunity Employer (EOE) M/F/D/V.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. Molina Healthcare offers a competitive benefits and compensation package.
Bring your passion and talents and together we can make a difference in the lives of others. If you are seeking a meaningful opportunity in a team-oriented environment, come be a part of a highly engaged workforce dedicated to our mission. Molina Healthcare is a nationwide fortune 500 organization with a mission to provide quality healthcare to people receiving government assistance. Pay Range: $41,264 - $80,465 a year* *Actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Molina Healthcare is an Equal Opportunity Employer (EOE) M/F/D/V. To all current Molina employees: If you are interested in applying for this position, please apply through the intranet job listing.
May provide feedback and suggestions to product development.
Defines strategy for effective communication. Analyses user information requirements including understanding the user experience in relation to company products.
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