Clinical Documents Coordinator

**Job Overview:** Clinical Documentation Compliance ExpertClinical Professionals Limited is seeking a highly skilled Clinical Documentation Compliance Expert to join our team. In this role, you will play a critical part in ensuring compliance with regulatory requirements by developing and implementing effective clinical documentation policies and...

Clinical Professionals Limited is seeking a skilled Regulatory Documents Coordinator to support our Regulatory Affairs Operations department in White City, West London. As a key member of our team, you will contribute to the implementation of Regulatory Records Management.Responsibilities:Provide audit support related to RA records managed by RA Operations,...

We are looking for a highly motivated Director of Clinical Documentation to join our team at Warman O'Brien.In this role, you will be responsible for overseeing the preparation and submission of clinical study documentation, ensuring accuracy and regulatory appropriateness.Key Responsibilities:Developing and implementing processes to ensure accurate and...

Job SummaryWe are seeking a highly skilled and motivated individual to join our team at WEP Clinical Inc. as a Clinical Trial Specialist. In this role, you will provide operational and administrative support to the clinical research team, working closely with the project management team to ensure the successful management of Expanded Access Programs (EAP),...

About the PositionWe are seeking a highly skilled Clinical Documentation Expert to join our team at Ipsen Pharma. In this role, you will be responsible for creating high-quality clinical documentation content, working closely with cross-functional teams to ensure timely delivery of projects.Key Responsibilities:Develop and manage complex clinical...

MMS is a dynamic and innovative CRO that supports the pharmaceutical, biotech, and medical device industries. We are seeking a talented Medical Writer to join our team and contribute to the development of high-quality clinical documents.Job SummaryThe Medical Writer will be responsible for writing and editing clinical development documents, including...

Clinical Documentation ManagerWe are seeking a highly experienced Clinical Documentation Manager to join our medical writing team at CM Consulting.About the Role:This role involves managing complex documentation projects, including clinical evaluation reports, across various therapeutic areas, such as oncology, rheumatology, haematology, diabetes,...

About the JobWe are seeking a skilled Documentation Coordinator to join our project team at Assystem GmbH in Warrington.In this role, you will be responsible for managing and coordinating documentation throughout the project lifecycle, ensuring compliance with regulatory requirements, and developing effective document management procedures.Developing and...

About the Job:We are currently recruiting for a Clinical Trials Coordinator to join our research team at Imperial College Healthcare NHS Trust. The successful candidate will be responsible for coordinating and managing clinical trials for investigational medicinal products, working closely with leading investigators and clinical research fellows.This is an...

We are currently working with a leading residential developer in South West London, seeking an experienced Document Coordinator to join their team.The ideal candidate will have a proven track record as a Document Controller for a construction sector business, with excellent communication and project coordination skills.Salary: £40,000 - £60,000 per annum,...

Novartis Farmacéutica is guided by its purpose: to reimagine medicine to improve and extend people's lives. We are seeking a talented Clinical Document Publisher to join our Regulatory Operations Team.About the JobThis role involves producing high-quality clinical deliverables and global submission outputs per agreed timelines and in compliance with...

Company Overview:Welcome to WEP Clinical Inc., a leading provider of expanded access programs, named patient programs, and clinical trial supplies. With over 15 years of experience in distributing products to over 120 countries worldwide, we have established ourselves as a trusted partner for sponsors and patients alike.Salary: The estimated salary for this...

Job SummaryWe are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at The Royal Marsden NHS Foundation Trust. This is a fantastic opportunity for an individual with excellent administrative skills and experience in clinical trials to make a real difference in the lives of patients.The successful candidate will be...

At Novartis, we reimagine medicine to improve and extend people's lives. As a Clinical Documentation Specialist, you will play a critical role in ensuring the quality of clinical trial documents.The estimated salary for this position is around $110,000 per year, depending on location and experience.About the JobResponsible for timely assessment of quality...

Job DescriptionWe are seeking a highly skilled and motivated Clinical Project Coordinator to join our team in London. As a key member of our Clinical Trial Management team, you will be responsible for coordinating and managing clinical trials from start to finish.Responsibilities:Coordinate and manage clinical trials, including preparing and submitting...

Job Description:We seek a skilled Clinical Documents Writer to join our team for a 3-month fixed-term contract. As a Medical Writer, you will translate complex scientific and clinical information into clear and concise documents, adhering to regulatory guidelines. Your primary responsibility will be to communicate medical and scientific information to...

About MMSMMS is an innovative data-focused Contract Research Organization (CRO) supporting the pharmaceutical, biotech, and medical device industries with a proven scientific approach to complex trial data and regulatory submission challenges.With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating and has been...

Job DescriptionWe are seeking a highly skilled Clinical Document Manager to join our team at Novartis. This role will be responsible for the delivery and oversight of CSR appendices authoring, formatting, compilation, and publishing required for regulatory submissions.Key ResponsibilitiesDrive implementation of CDGM initiatives, projects, and process...

Job OverviewRichmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and contribute to the development of life-changing therapies.About the RoleWe are seeking an...

About WEP Clinical Inc.We are a leading provider of clinical trial supplies and expanded access programs. Our mission is to improve patient outcomes by providing innovative solutions for pharmaceutical companies.Our Services:Expanded Access Programs (EAPs)Named Patient Programs (NPPs)Clinical Trial Supplies (Comparator & Ancillaries)Wren Nursing (Clinical...