Senior Clinical Document Specialist
3 days ago
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 apply.
Responsibilities:
- Author and compile CSR appendices according to ICH E3.
- Develop and implement submission readiness processes and strategies.
- Serve as Subject Matter Expert on CSR appendices training materials and tracking tools.
Requirements:
- 5 years of experience in clinical development/clinical operations or similar business area.
- 2-3 years of working experience with document management systems.
- Excellent understanding of system structures and generic document management functionality.
Salary: $90,000 - $120,000 per annum
We offer a competitive salary, comprehensive benefits package, and opportunities for career advancement.
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Senior Medical Editor
3 weeks ago
London, Greater London, United Kingdom Lifelancer Full timeJob Title:Senior Medical Editor - Clinical Document SpecialistAbout the Role:We are seeking an experienced Senior Medical Editor to join our team as a Clinical Document Specialist. This role will be responsible for ensuring the quality and accuracy of clinical documents intended for submission to health authorities worldwide.Key Responsibilities:Document...
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Clinical Documentation Compliance Expert
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London, Greater London, United Kingdom Clinical Professionals Limited Full time**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...
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Clinical Development Document Specialist
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London, Greater London, United Kingdom MMS Holdings Inc Full timeJob 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...
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Clinical Documentation Specialist
3 weeks ago
London, Greater London, United Kingdom Richmond Pharmacology Full timeJob 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...
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Clinical Documentation Specialist
15 hours ago
London, Greater London, United Kingdom Novartis Full timeAt 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...
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Clinical Documentation Specialist
3 days ago
London, Greater London, United Kingdom Richmond Pharmacology Full timeJob 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...
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Clinical Document Management Specialist
4 weeks ago
London, Greater London, United Kingdom Novartis Full timeAt 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...
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Clinical Document Specialist
4 weeks ago
London, Greater London, United Kingdom Lifelancer Full timeJob DescriptionLifelancer is a talent-hiring platform connecting professionals with opportunities in pharma, biotech, and health sciences.We are seeking a Clinical Document Specialist to support our global clients in the biotech industry. The successful candidate will be responsible for quality control review of clinical documents intended for submission to...
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Regulatory Documentation Specialist
3 days ago
London, Greater London, United Kingdom Actalent Full timeWe are seeking a highly skilled Regulatory Documentation Specialist to join our team in the UK. As a Senior Medical Writer, you will play a crucial role in producing high-quality regulatory documentation for the international pharmaceutical industry.With a strong background in medical writing and a deep understanding of regulatory requirements, you will work...
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Clinical Document Governance Specialist
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London, Greater London, United Kingdom Healthcare Businesswomen's Association Full timeWe 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...
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Senior Regulatory CMC Document Specialist
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London, Greater London, United Kingdom RBW Consulting Full timeJob Title: Senior Regulatory CMC Document SpecialistAt RBW Consulting, we are seeking a highly skilled Senior Regulatory CMC Document Specialist to join our team. In this pivotal role, you will be instrumental in preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical...
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Clinical Research Documentation Specialist
6 days ago
London, Greater London, United Kingdom Publicis Groupe UK Full timeClinical 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...
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Clinical Documentation Expert
4 weeks ago
London, Greater London, United Kingdom George Buckland Life Sciences Recruitment Full timeWe are seeking a highly skilled Clinical Documentation Expert to join our team at George Buckland Life Sciences Recruitment. As a Clinical Documentation Expert, you will be responsible for creating accurate and comprehensive clinical documentation, focusing on the therapeutic areas of Oncology and Endocrinology.In this role, you will work closely with a...
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Clinical Transformation Specialist
6 days ago
London, Greater London, United Kingdom First Clinical Ltd Full timeJob TitleClinical Transformation SpecialistAbout UsFirst Clinical Ltd is a leading healthcare organisation seeking an experienced Clinical Transformation Specialist to join our team.Salary and BenefitsThe successful candidate can expect a competitive salary of around £120,000 per annum, depending on experience.Job DescriptionWe are looking for a highly...
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London, Greater London, United Kingdom Barrington James Full timeBarrington James, a leading clinical trials sector organisation, is seeking a highly skilled Senior Manager of Clinical Documentation and Compliance. This senior leadership position offers the opportunity to drive business growth and advance medical innovation.The successful candidate will oversee the preparation and delivery of high-quality regulatory...
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Senior Clinical Content Specialist
4 weeks ago
London, Greater London, United Kingdom Calyx Full timeCalyx offers an attractive compensation package, estimated to be around $80,000 - $110,000 per year.As a Senior Clinical Content Specialist at Calyx, you will play a critical role in the development, editing, and finalization of study-specific documents. These documents may be used for regulatory submissions, and you will manage them through to finalization...
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Clinical Document Specialist
6 days ago
London, Greater London, United Kingdom Only Medics Full timeA 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...
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Clinical Product Specialist
15 hours ago
London, Greater London, United Kingdom Clinical Professionals Limited Full timeClinical Professionals Limited is a leading provider of clinical services. We are currently seeking a highly skilled Clinical Product Specialist to join our team in London.Job Description:The primary aim within this role will be to use your clinical knowledge and experience when liaising with NHS stakeholders, HCPs, KOLs and advocates across the territory to...
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Regulatory Document Specialist
3 days ago
London, Greater London, United Kingdom Stemline Therapeutics Full timeJob DescriptionWe are looking for a highly skilled Regulatory Document Specialist to join our team in the United Kingdom. As a remote opportunity, this role offers a competitive salary and a chance to work on critical clinical documents.The successful candidate will have a minimum of 5-10+ years of experience in regulatory medical writing, with a proven...
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Clinical Leadership Specialist
6 days ago
London, Greater London, United Kingdom First Clinical Ltd Full timeAbout the RoleWe are looking for a highly skilled Clinical Leadership Specialist to join our team at First Clinical Ltd.The successful candidate will have a strong track record of project management, including experience in sourcing and providing cover for clinic activity, preparing remedial action plans (RAP) reports and following-up patient backlogs and...