Mentors and leads less experienced medical writers on complex projects, as necessary. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. We translate unique clinical, medical affairs a...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatisti...
Build strong relationships with Creative, Medical, Account, and Client brand teams, such that each group identifies you as the holder of all copy, editorial and clinical knowledge for the brand. Partner with Creative, Medical/Strategy, Account and Client teams to ensure copy that advances creative b...
Essential Functions Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include: Clinical study protocols and protocol amendments Clinical study reports (CSR) Investigator brochures (IB) Informed consent and assent forms Lay summaries ...
THE COMPANY Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies. THE WORK Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several dif...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatisti...
THE COMPANY Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies. THE WORK Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several dif...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, ...
Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and Managed Care Liaisons), and standard or complex medical information responses. As needed, provide medical ...
You're an established Senior Medical Writer looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, uni...
Responsibilities: Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias Write and edit clinical development d...
Clinical Communications, you will be working closely with an internal team dedicated to producing educational medical/scientific content (eg, peer-reviewed manuscripts, slide decks, video-based learning) for oncology care. You will have an opportunity to develop content on topics spanning the oncolo...
Team Mentoring, Motivating, Training and Oversight for a team of Project Managers, Clinical Research Associates (CRAs), Clinical Trial Associates (CTAs). Manage and track study budget, project milestones, and timelines throughout the life of the study and perform contract reconciliation at study end...
The CClient Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical...
This role will develop and lead all medical affairs activities ensuring partnership within the team (medical strategy, scientific communications and publications) all key Medical Affairs functions (Medical Excellence, HEOR, Field Medical, Medical Information) as well as maintaining a high-level cros...
We’re looking for a Senior Director of Medical Affairs to join a growing Big Pharma firm based out of Princeton, NJ! In this hybrid role, you’ll work cross-functionally with key internal players (RWE, HEOR, Medical Excellence, etc. Medical Affairs experience within the dermatology space. If this isn...
Project Managers have the freedom to manage their projects that suit their management style. Experience in project and task management is also required including coordination with management, clients, contractors, and project teams. Our team is known for developing and successfully implementing cutt...
We are seeking a Technology Systems and Support Coordinator to oversee and manage activities, projects, and processes to support digital innovation and transformation initiatives. Supports the implementation through project management, configuration review, testing, trouble shooting and training to ...
Content Management - Proofreader. As a Content Management - Proofreader. ...
The Global Segment Project Manager (PM) manages priority global Innovation and Life Cycle Management projects in support of Kenvue's and assigned Segment's Strategic Plan, Objectives and Key Results (OKRs). Global Segment Project Manager. In service of assigned Brand Development Team(s) (BDT), provi...
Our Global Fortune 500 client is looking for a Technical Writer with the following skills and qualification:. Good experience in writing manuals, technical documentation, job aids, SOPS as well as SDLC documentation. Experience preferred in writing documentation, user guides, technical job aids, PPT...
The Project Manager, Global Supply Chain (GSC) Strategy & Business Operations (S&BO), Strategic Initiatives is responsible for leading the planning and execution of high-priority and complex GSC cross-functional projects and/or programs. Experience in project/program management of complex projects i...
Job Description: Senior Proofreader Job Description. ...
Job Posting Title Lead Digital Writer/Editor Date Wednesday, January 10, 2024 City Princeton State NJ Country United States Working time Full-time. Develop and manage client editorial guidelines for tone and style, and ensure they are followed. ...