Global Clinical Document Manager

**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...

We are looking for a highly skilled Clinical Documents Coordinator to join our team at Novartis Farmacéutica.About the JobThis is a challenging role that requires strong technical skills and attention to detail.Responsible for preparing, publishing, and reviewing clinical documents and global regulatory submissions.Work closely with cross-functional teams...

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...

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...

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,...

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...

A global pharmaceutical organisation specialising in oncology, immunology and rare diseases is seeking a Medical Document Reviewer to join their medical affairs team.Core Skills and Experiences Required:Experience working in a Medical Affairs teamAbility to review documents from various teams including customer support, marketing, regulatory, clinical,...

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...

A leading global pharmaceutical company in oncology, immunology, and rare diseases is seeking a highly skilled Medical Document Reviewer to join their medical affairs team. This exciting role offers an opportunity to work with a talented team of professionals who are dedicated to delivering innovative solutions for patients worldwide.Key...

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...

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 OverviewThis role within Global Clinical Oncology R&D will serve as a clinical sciences leader on global oncology studies and contribute to program-level activities. The ideal candidate will have experience in data analysis and interpretation, scientific publications, and study design, as well as experience in a pharmaceutical industry or CRO environment...

Resourcing Life Science is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. Our client offers a full-service solution encompassing clinical & non-clinical development, peri-approval & market access.About the JobWe are looking for a Global Clinical Project Manager in London to lead cross-functional project teams globally....

**Job Description:**As a Document Management Systems Coordinator at EarthStream Global, you will play a key role in ensuring the smooth operation of our document management systems.Estimated Salary: $80,000 - $110,000 per year.Main Responsibilities:Implement and maintain document management systems and processes.Collaborate with stakeholders to ensure...

Job Overview:We are recruiting a Senior Clinical Trials Manager to join our team at CCS-Global. The successful candidate will have a strong background in clinical research and excellent leadership skills.About CCS-Global:CCS-Global is a dynamic organization dedicated to advancing clinical research and delivering positive patient outcomes. We are committed to...

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 Description:Global Clinical Operations ManagerWe are looking for a seasoned Global Clinical Operations Manager to oversee the management of clinical trials across various regions. As a key member of our team, you will be responsible for ensuring the successful execution of trials from start-up to database lock and trial closure.Main...

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 DescriptionThe Global Pharmacovigilance Manager will be responsible for managing the collection, processing, and reporting of adverse event reports for all Novartis products.Responsibilities:Manage the collection, processing, documentation, reporting, and follow-up of all adverse event reportsTranscribe, translate, and enter data from source documents...

Key ResponsibilitiesThe Head of Clinical Documentation will be responsible for providing senior-level expertise and management for our client's medical writing team.This is a hybrid role in Central London, requiring applicants to be prepared to work on-site four days per week.Key responsibilities include:Fulfilling medical writing and regulatory...