- Baptist Memorial (Memphis, TN)
- Summary The Technical Communications Writer - Senior uses technical communications and knowledge management skills to document knowledge and coach knowledge ... may need to include multiple versions based on user needs. Responsibilities The Technical Communications Writer -Senior will: * Work with SR IT Communications… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …pharmaceutical services. The Senior Proposal Writer Manager will serve as the lead writer for the Global Business Development (GBD) team, including: drafting ... disabilities. Brief Job Overview USP seeks a Senior Proposal Writer Manager to serve as a key member of...In collaboration with SMEs, from capture to proposal development, lead technical proposal writing processes. * Interprets… more
- The Cigna Group (Bloomfield, CT)
- The RFP Content Management Writer plays a critical role within RFP Strategy & Operations for Cigna's US Commercial markets. This individual is responsible for ... impact the overall new business and retention sales process. The Content Management Writer is responsible for partnering with subject matter experts (SMEs) that span… more
- Pfizer (Pearl River, NY)
- …of clinical trials by applying extensive expertise and in-depth knowledge of clinical research to lead global clinical research programs and registration ... to clinical research programs. The clinician medical monitor applies technical /scientific expertise to resolve problems regarding the clinical components of… more
- Pfizer (Bothell, WA)
- …by line management. + As necessary, act as clinician for Phase I studies or clinical lead / research project lead for specific drug development projects. ... clinical development programs. You will be the primary Clinical Pharmacology Lead providing clinical ...reporting of the CP study. Share responsibility with Medical Writer , for overall content and accuracy of study report… more
- Pfizer (Pearl River, NY)
- …delivery of top-line report in collaboration with study statistician, and delivery of clinical study report in collaboration with medical writer and accountable ... for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of...review of cumulative safety data with the safety risk lead . As appropriate, the clinician medical monitor may delegate… more
- Institute for Medical Research (Durham, NC)
- …research lab. Grants and Contracts Coordinator will report to the Proposal and Grant Writer Team Lead or designee. The successful candidate will have the ... Contracts Coordinator to assist with pre-award research planning for clinical research studies conducted by the Principal Investigator, Dr....under the direct supervisor of the Proposal and Grant Writer Team Lead . The prior statements describe… more
- Pfizer (Collegeville, PA)
- …delivery of top-line report in collaboration with study statistician, and delivery of clinical study report in collaboration with medical writer and accountable ... towards providing medical and scientific expertise and oversight for Clinical Trials. + The clinician medical monitor may be...review of cumulative safety data with the safety risk lead . + As appropriate, the clinician medical monitor may… more
- J&J Family of Companies (Columbus, OH)
- …some mentorship from functional management and clinical team, as needed. + If a lead writer for a program: Be the primary point of contact and champion for ... Authoring experience with investigator brochures, clinical study protocols, and clinical study reports. Experience with common technical document summaries… more
- University of Colorado (Aurora, CO)
- …position will help coordinate external communications and social media accounts, act as lead writer for the unit's bi-monthly newsletter, and assist with complex ... accredited institution. + Substitution: A combination of education and related technical /paraprofessional experience may be substituted for the bachelor's degree on… more