A staffing agency is in need of a Work at Home Senior Pharmaceutical and Medical Writer. Candidates will be responsible for the following: Writing clinical protocols and clinical study reports (CSRs) Writing investigational pediatric study plans (ISPS) and pediatric investigational plans (PIPs)
Supporting the medical writing team in the development of protocol design as well as CSR review and input. Interacting with Business Development for all proposal development support related to therapeutics for Oncology. Applicants must meet the following qualifications:
Read, write and speak fluent English; fluent in host country language required. Must be a licensed health-care professional (i. e. , registered nurse); or equivalent work experience. Read, write and speak fluent English; fluent in host country language required.
Ability to read, write and speak proficiently in both English and Spanish. Clinical experience in adult acute care environment. Must have accessibility to hardwired high speed internet with minimum speeds of 10Mx1M for a home office. Case Management Experience.
A staffing agency is in need of a Telecommuting Principal Medical Writer in Chicago. Candidates will be responsible for the following: Serving as medical writing lead on more complex scientific publications or clinical regulatory documents.
Attend and/or present at investigator, internal and external project team meetings. 3+ years of experience writing pharmaceutical or health-related documents. Must be a licensed physician. Experience using computerized systems. Significant clinical trial experience.
A staffing company is seeking a Telecommute Senior Medical Writer. Core Responsibilities Include: Author clinical summaries. Conduct over-the-counter/OTC applications Benefit Risk assessments. Provider overview of 2. 5, briefing books, and ISS (integrated safety summaries)
Experience leveraging patient-level healthcare data (claims, EHR, etc. ) to support commercially oriented business questions such as forecasting and segmentation. Experience developing new business and identifying add-on work. Excellent writing and presentation skills.
Must have experience monitoring Hematology/Oncology TrialsPhase I experience required. Read, write and speak fluent English; fluent in host country language required. Knowledge of ICH and local regulatory authority regulations. 4+ years of clinical monitoring experience required.
3+ years of experience in system and data integration. Proficient in the use of MS Office including Word and PowerPoint. Writes clearly and concisely and demonstrates ability to simplify description of complex subjects. Actively pursues continuous quality/process improvement.