Clinical Documentation Expert

Job Title: Associate Director of Medical WritingJob Overview:Clinical Professionals Limited is seeking an experienced Associate Director of Medical Writing to lead our medical writing activities and serve as an expert Medical Writer. The successful candidate will be responsible for planning, developing, and writing clinical and regulatory documents to...

Worldwide Clinical Trials is seeking a CLINICAL CONTENT EXPERT - EUROPE to create customized solutions that meet the unique needs of our clients.As a key member of our team, you will develop comprehensive clinical trial plans and solve problems quickly for our customers. With a strong focus on cardiovascular, metabolic, neuroscience, oncology, and rare...

At Novartis, we're committed to delivering exceptional results and fostering a culture of innovation. As a Clinical Document Management Specialist, you'll play a critical role in shaping our clinical document management systems, processes, and standards.Job Summary:We're seeking an experienced professional with expertise in clinical documentation practices...

We are seeking a highly skilled Clinical Document Governance Specialist to join our team at the Healthcare Businesswomen's Association. This is a hybrid role that can be based in Dublin or London offices, with an expectation of being in the office 12 days/month.Job DescriptionThe successful candidate will be responsible for ensuring delivery and oversight of...

A leading pharmaceutical organisation is seeking a Medical Document Reviewer to join their medical affairs team.Key Responsibilities:Review and approve documents from various teams, including customer support, marketing, regulatory, clinical, scientific, and medical.Collaborate with the AQP for medical affairs teams to ensure seamless document approval...

Job Description:We are seeking a skilled Documentation Specialist to join our team at J Bandy Consulting.The successful candidate will be responsible for producing high-quality technical documentation that is easy to understand and accessible to various audiences. This includes creating, maintaining, and distributing documentation, collaborating with teams...

**Job Overview**Clinical Professionals Limited is seeking an experienced Digital Content Management Expert to join our Global Marketing Operations team.As a key member of the team, you will be responsible for ensuring that digital content is managed efficiently across various channels and platforms.**Salary & Benefits**The successful candidate can expect a...

Job Title: Document Automation ExpertAbout the Role:We are seeking a skilled Document Automation Expert to join our team at Jameson Legal. As a Document Automation Expert, you will work closely with clients to understand their needs and requirements, providing expert advice and recommendations to enhance and optimize templates.Key...

MMS is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Key ResponsibilitiesCritical Evaluation and Analysis: The Medical Writer will critically evaluate, analyze, and interpret the medical...

**About the Role:**Clinical Professionals Limited is recruiting a talented Device Design Expert to join our team.Job Description:The successful candidate will be responsible for designing and developing medical devices that meet the required standards. This includes creating technical design documents, generating test protocols, performing product testing,...

About the RoleWe are seeking a highly skilled and experienced Senior Interim Manager to join our First Clinical Ltd team. This is an exciting opportunity for a qualified and dedicated professional to lead and deliver quality improvement and service development projects in a dynamic healthcare environment.Key ResponsibilitiesDrive quality improvement...

Job Title: Clinical Development Document SpecialistAbout MMS Holdings Inc.MMS Holdings Inc. is a global leader in contract research organization services, supporting the pharmaceutical, biotech, and medical device industries with data-focused solutions. Our mission is to deliver high-quality clinical development documents that meet rigorous regulatory...

Translate Plus Job OpportunityWe are looking for a skilled Medical Writer, fluent in Turkish, to work on various projects within the healthcare industry. The ideal candidate will have experience in writing clinical study protocols, reports, and regulatory documents.Key Responsibilities:• Prepare high-quality clinical study protocols and reports• Edit and...

Technical Documentation ExpertWe're seeking a skilled Technical Documentation Expert to join our team in London, United Kingdom.Job Title: Technical Documentation ExpertSalary: £55,000 - £75,000 per annumContract Type: PermanentAbout the Role:This is an exciting opportunity for a motivated and experienced Technical Documentation Expert to work with our...

Triple West Medical invites applications from experienced Clinical Experts who wish to take on the challenge of providing exceptional patient care as a Rheumatologist in our esteemed University Hospital located in the East of England. With a population of over 300,000 residents, our hospital provides a wide range of general acute services, as well as...

Associate Director, Medical WritingJob Type: PermanentLocation: Oxford, UK – Hybrid/RemoteRemuneration: Attractive salary and packageAn exciting opportunity for an experienced Medical Writer to join a growing biotechnology company who are at the forefront of Oncology innovation within Radiopharmaceuticals.As an Associate Director, Medical Writing, you will...

At Publicis Groupe UK, we are seeking a highly skilled Medical Writer to join our team. As a Clinical and Regulatory Expert, you will be responsible for translating complex scientific and clinical information into clear and concise documents for our clients in the healthcare and pharmaceutical industries.Clinical and Regulatory Writing:Prepare and edit...

Company OverviewWe are Worldwide Clinical Trials, a global team of over 3,500 experts who take pioneering approaches and implement them with quality and excellence. We believe in making a world of difference for patients and their caregivers.

Job Title: Clinical Commissioning StrategistEstimated Salary: £80,000 - £100,000 per annumAbout the Role:We are seeking an experienced Clinical Commissioning Strategist to join our team at First Clinical Ltd. As a key member of our commissioning team, you will be responsible for developing and implementing effective commissioning strategies to improve...

Job DescriptionThis role involves providing quality control review of clinical documents intended for submission to health authorities worldwide. The Senior Medical Editor will copyedit/proofread, format, and verify data content in clinical documents in accordance with SOPs and processes to ensure documents meet required standards.Responsibilities:Perform QC...