Trabajos Writing & Editing en SandownCrear alertas

Are you looking for an interpreter job in Ryde, Isle of Wight?.Do you want flexible hours with competitive rates?.We are urgently recruiting for freelance interpreters to work within various settings such as the NHS, Local Authorities, Police, Probation and other public and private organisations.Est

Are you looking for an interpreter job in Isle Of Iona?.Do you want flexible hours with competitive rates?.We are urgently recruiting for freelance interpreters to work within various settings such as the NHS, Local Authorities, Police, Probation and other public and private organisations.Establishe

Regulatory Medical Writing Lead. Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years' experience in managing/supervisin

Online English Writing and Analysis Teacher - All Levels.

We are looking for experienced Directors of Regulatory Writing with previous experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency to join our team and help us to build on our continuing success. At Complete Regulatory,, we provide class-leading writing

Evidence of successful proposal writing, from start to finish, as well as experience with writing concise reports. ProVeg International is looking for a Grant Writing Manager to join their team. The role of the Grant Writing Manager at ProVeg is to provide excellent and compelling fundraising conten

We have writing vacancies across multiple levels;. Experience in a medical writing role as part of a healthcare comms agency.

Extensive experience in Medical Writing, writing regulatory reports and clinical/scientific documents in a medical/pharmaceutical field. We have an exciting new opportunity for a Medical Writing Manager to lead and develop the medical writing function in the Centre for Drug Development (CDD). Drive

Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years' experience in managing/supervising activities associated with the

Most of the writing in Source takes a specific form: book reviews, exhibition reviews or texts introducing sets of pictures, so these would be good models to follow. But we are also interested in others forms of writing so if you want to submit something in a different form, then please do. We enjoy

Technical expert on all document types produced by medical writing. Please note this role is a senior role within the business, so you MUST have extensive experience in RA medical writing and have excellent communication skills. Sign in to set job alerts for “Manager Medical Writing” roles.

Technical expert on all document types produced by medical writing. Please note this role is a senior role within the business so you MUST have extensive experience in RA medical writing and have excellent communication skills. Regulatory Medical Writing Lead, west midlands.

Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in the pharmaceutical industry, with 2-5 years' experience in managing/supervising activities associated with the creation of regulated documents in the pharmaceutical industry. Technical expert on all document type

Online English Writing and Analysis Course Developer - All Levels. Successful candidates will be cooperating with our in-house course creation team to write, test, and revise courses with topics ranging from elementary writing to analyzing Shakespeare and everything in between.

We are seeking experienced Directors of Regulatory Writing with a background in regulatory or medical writing within the pharmaceutical industry or agencies. You will lead complex submissions, guide team members, and serve as a trusted partner to our clients, demonstrating strategic thinking to ensu

Senior Manager, Regulatory Medical Writing, west midlands. Senior Manager, Regulatory Medical Writing. Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams.

Medical Writing Vacancies (Multiple Levels), england. We have writing vacancies across multiple levels;. Experience in a medical writing role as part of a healthcare comms agency.

Medical Writing Manager / Lead. Oversee the end-to-end management of medical writing projects, including planning, timeline management, stakeholder coordination, and delivery of final documents. Proven experience in a senior or principal medical writing role.

Please note this role is a senior role within the business so you MUST have extensive experience in RA medical writing and have excellent communication skills. Writing/Editing, Strategy/Planning, and Science. Sign in to set job alerts for “Manager Medical Writing” roles.

Writing Experts for AI Training - English. Exceptional writing skills and creative mindset.

We seek experienced Directors of Regulatory Writing with a background in pharmaceutical regulatory or medical writing agencies. You will lead complex submissions, guide team members, and serve as a trusted partner to our clients, demonstrating strategic thinking and ensuring effective medical writin

Please note this role is a senior role within the business so you MUST have extensive experience in RA medical writing and have excellent communication skills. Regulatory Medical Writing Lead, newcastle-upon-tyne, tyne and wear. Regulatory Medical Writing Lead.

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. May input into and deliver presentations on Medical Writing to other IQVIA groups. In dep

Regulatory Medical Writing Lead. Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years' experience in managing/supervisin

Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. Technical expert on all document types produced by medical writing. Regulatory Medical Writing Lead.

Technical expert on all document types produced by medical writing. Please note this role is a senior role within the business, so you MUST have extensive experience in RA medical writing and have excellent communication skills. Senior Manager, Regulatory Medical Writing, bedford.

Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years' experience in managing/supervising activities associated with the creation of regulated documents in the pharmaceutical industry. Technical expert on all document types pr

Drive the continuous review of Medical Writing processes and external systems that support Medical Writing (e. Extensive experience in Medical Writing, writing regulatory reports and clinical/scientific documents in a medical/pharmaceutical field. We have an exciting new opportunity for a Medical Wr

In this article, AMDAS will provide you with expert CV writing tips to help you create a standout resume that catches the attention of UK employers. Before you start writing your CV, thoroughly analyze the job description provided by AMDAS or any other prospective employer. Expert CV Writing Tips fo

Regulatory Medical Writing Lead, bedford. Regulatory Medical Writing Lead. Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams.