Clinical Documentation 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...

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...

Role Overview:We are seeking a highly organized and detail-focused Document Management Coordinator to join our team at Walkers Documentation Firm T Shirts.In this role, you will be responsible for providing administrative support to our sales team, including typing invoices, answering telephones, and speaking with clients about their confirmed orders and L/C...

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...

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...

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...

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...

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...

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...

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...

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 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 OverviewRichmond Pharmacology is a leading Contract Research Organisation specialising in early-phase clinical trials. We are seeking a highly skilled Medical Writer to join our team in London Bridge.We offer a competitive salary of £45,000 - £60,000 per annum, plus benefits including private medical and dental insurance, pension scheme, and 25 days...

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...

Clinical Evaluation Report Writer Job DescriptionWe are seeking a Medical Writer, native Swedish speaker to join our team for 3 months. The successful candidate will have expertise in healthcare and pharmaceutical industries by translating complex scientific and clinical information into clear and concise documents.Job Responsibilities:Prepare and edit...

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...

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...

About the Role:We are seeking a skilled CORPORATE RESPONSIBILITY MANAGER to join our team at Novartis. In this role, you will be responsible for delivering high-quality CSR appendices while ensuring compliance with regulatory requirements. If you have a passion for clinical document management and regulatory affairs, we encourage you to...

About the RoleWe are looking for a highly motivated Clinical Programme Manager to lead the development and implementation of new clinical programmes at First Clinical Ltd. As a key member of our clinical team, you will work closely with clinicians, directors, and other stakeholders to design and deliver high-quality clinical services.The ideal candidate will...

Job OverviewFirst Clinical Ltd is seeking a highly skilled Senior Clinical Operational Manager to lead our clinical teams. With over 20 years of experience in healthcare management, this professional has an MBA and Prince2 Practitioner status.The ideal candidate will have strong operational management skills and experience in managing clinical sites, patient...