Principal Medical Writer - Morrisville, NC

++As principal medical writer on clinical study or regulatory project teams, you provide scientific writing, regulatory guidance and technical expertise in the writing production and review of high quality complex documents ensuring that clinical data is presented compliant with ...

We are looking for a Senior Medical Writer with strong expertise in late Phase Protocol and CSR writing. Experience with authoring of additional documents such as NDA, IND, IB, DSUR, RMP, ...

Sr Medical Writer - Medical Device + Regulatory Documents - Remote Based Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical medical affairs and commercial insights into outcomes to ...

The Medical Writer role is responsible for writing and editing manuscripts and other medical communications on clinical studies and/or scientific reports including special summaries from raw data for submission to regulatory agencies or for in-company use, · Leads the clear and a ...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. · ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with but to make us easier to work for. · Mentors and leads less experienced medical writers on complex projects as necessary. · ...

Principal Medical Writer. · Acts as Lead Medical Writer on any type of writing project and can advise others on any type of document. · Negotiates timelines and discusses/resolves customer comments. · Bachelor's Degree Bachelor's Degree in life sciences related discipline or rela ...

The incumbent will assist in the creation, review and revision of documents (SOPs, forms, jobs aids, training material etc.) and other manufacturing department documents. · ...

Join an industry-changing company that is reinventing the way we develop and commercialize drugs. Senior medical writer on clinical study or regulatory project teams. Plans and coordinates report-writing activities with dependent staff roles to ensure satisfactory completion of a ...

We are seeking a Principal Medical Writer specializing in Chemistry, Manufacturing and Controls (CMC) for immediate opening. The ideal candidate will support our growing company in producing regulatory documentation for the international pharmaceutical industry. · Applicants must ...

We are seeking a CMC writer experienced in interpreting technical data from manufacturing, quality control, and analytical development teams to create comprehensive, compliant, · and accurate CMC dossiers for regulatory authorities.Write, · edit, · and review complex CMC regulato ...

+Acts as Lead Medical Writer on any type of writing project and can advise others on any type of document. · +Communicates various medical writing topics to a broad audience and identifies appropriate parties to be included. · Essential FunctionsTake a leading role in preparing a ...

We are hiring Senior/Principal Medical Writers to support our growing company in producing regulatory documentation for the international pharmaceutical industry. · ...

Trilogy Writing & Consulting is hiring Senior/Principal Medical Writers to support the writing and coordination of successful documentation across a broad spectrum of therapeutic areas. · ...

A medical editor is responsible for improving and ensuring the quality of compliance of written deliverables through copyediting, quality review, and document management. · ...

+h2>Job summary · Join Relias to create up-to-date content based on industry best practices for healthcare organizations. · Research and plan content based on learning objectives. · Create engaging content using instructional design principles. · ...

The Technical Writer supports the manufacture of Phase 1, 2 and3 for clinical supplies and commercial supplies working closely with quality and operations management. · The Role:Perform investigations; write problem reports prior to QA review;Create and revise standard operating ...

We are passionate about developing our people, through career development and progression; · We are committed to our Total Self culture – where you can authentically be yourself. · We are continuously building the company we all want to work for and our customers want to work wit ...

The Accountant II is responsible for all areas relating to month end close and financial reporting. This position will be responsible for developing and maintaining accounting principles, practices, and procedures to ensure accurate and timely financial statements. · This positio ...

Actalent is seeking a Sr. GMP Technical Writer to be embedded onsite with a pharmaceutical or biotechnology client during the early stages of a new manufacturing facility build or major expansion. · This role will lead and own the documentation workstream, partnering closely with ...