Head of Clinical Documentation

**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...

Warman O'Brien is recruiting a Head of Clinical Documentation and Compliance to join our team in Central London. This role requires a strong understanding of regulatory requirements and the ability to lead a team of writers in the development of high-quality medical content.The successful candidate will be responsible for overseeing the preparation and...

About the Role:As a Head of Clinical Services, you will play a vital role in driving operational performance, financial management, governance, change, and business development across our Division. You will be responsible for delivering competing targets, including financial, quality, performance, productivity, and workforce targets.Key Requirements:Proven...

We are looking for a Head of Clinical Services Manager to lead our operational teams and drive excellence in service delivery.Key Responsibilities:Assist the Senior Management Team in driving operational performance, financial performance, governance, change and business development across the Division.Deliver a range of competing, challenging targets...

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 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...

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...

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,...

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...

We are seeking a dynamic and results-driven Head of Data Management to join our team at CTI Clinical Trial and Consulting Services. This is a fantastic opportunity to work with a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors.Job DescriptionThe successful candidate will...

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: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 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...

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 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...

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...

e-therapeutics plc is seeking an experienced Senior Director, Head of Clinical Operations to lead the development of global clinical programs and operations. As a member of our leadership team, you will play a key role in shaping the future of our company and contributing to the success of our RNAi therapies.About the RoleThe successful candidate will have...

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...

Job OverviewWe are seeking a highly skilled professional to fill the role of Head of Medical Writing and Regulatory Submissions at Barrington James. This senior leadership position offers a unique opportunity to lead and manage teams in a dynamic research-driven environment.The ideal candidate will have a strong background in medical writing and regulatory...