Regulatory Document Translator

Document Review and Translation ExpertAbout Our PartnershipPage Personnel Sales is working with a top-tier law firm in London to hire a skilled Document Review and Translation Expert for their Romanian Document Review team.The Perfect CandidateExcellent command of Romanian and English languages.Experience in document review, analysis, and translation.The...

We 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...

Job 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...

**Job Description:**We are seeking a highly skilled Regulatory Documentation Lead to join our team at Albion Rye Associates. The ideal candidate will have extensive experience in regulatory writing, clinical research, and leadership, with a strong understanding of regulatory requirements across all phases of development and pathways.Responsibilities:Prepare...

Richmond Pharmacology is a leading Contract Research Organisation (CRO) that specialises in early-phase clinical trials for pharmaceutical and biotechnology sponsors.We offer a competitive salary of £55,000 - £70,000 per annum, depending on experience, as well as benefits such as private medical insurance, pension scheme, and 25 days annual leave plus bank...

Key ResponsibilitiesWrite and review various clinical and regulatory documents such as clinical study protocols (CSPs), clinical study reports (CSRs), informed consent forms (ICFs), summary documents, advertising material and regulatory responses. Collaborate with other senior writers and sponsors to develop and execute communication plans. Ensure all...

Job Title: Senior Pharmaceutical WriterWe are seeking a detail-oriented and skilled technical writer to join our team as a Senior Pharmaceutical Writer. This is a fully remote position with occasional travel to our R&D Centre in Paris, France.In this role, you will be responsible for preparing and submitting high-quality CMC regulatory documents to support...

Senior CMC Regulatory Technical Writer:We are seeking an experienced Senior CMC Regulatory Technical Writer to join our team at RBW Consulting. In this role, you will play a critical part in developing and maintaining high-quality CMC regulatory documents to support registration activities.Key Responsibilities:Develop and maintain regulatory documentation,...

About the RoleWe seek an experienced professional to join our Investment Product and Fund Strategies (IPFS) group as a Regulatory Documentation Specialist. In this role, you will be responsible for creating, overseeing, and maintaining regulatory documentation for the WMF Global business.Responsibilities:Prospectus Cycles: Manage the end-to-end process for...

MMS Holdings Inc is a leading CRO that supports the pharmaceutical, biotech, and medical device industries with a data-focused approach to complex trial data and regulatory submission challenges.Job SummaryWe are seeking an experienced Regulatory Document Specialist to join our team. This role will involve critically evaluating, analyzing, and interpreting...

About the RoleAs a Regulatory Documentation Clerk at AWE, you will play a crucial role in supporting our Liabilities function. Your responsibilities will include coordinating leadership, regulatory, customer and/or technical meetings, ensuring that all necessary documentation is prepared and maintained.We offer a competitive salary of £45,000 - £60,000 per...

Role OverviewWe are seeking a highly skilled Regulatory Records Associate to join our team in London. The successful candidate will work on a 06-month contract, supporting the implementation of Regulatory Records Management.The hourly wage for this position is £28.48/hour.Duties and ResponsibilitiesSupport the Head of RA Ops Mergers and Acquisitions in...

Regulatory Documentation Specialist Job DescriptionThe primary function of this role is to oversee the management of regulatory documentation for company and project-related documents within our eQMS system.Key Responsibilities:Manage document lifecycle, including creation, review, approval, and archiving processes across the business.Oversee the maintenance...

Job Description: We are recruiting a highly skilled Medical Writer to join our team at Richmond Pharmacology. The ideal candidate will have at least 2 years of relevant clinical/regulatory medical writing experience and excellent written and verbal communication skills. Key Responsibilities: Develop diverse materials across various therapeutic areas,...

Job OverviewWe are seeking a highly skilled Senior Medical Writer to join our team in London, UK.The ideal candidate will have at least 3 years of experience writing regulatory documents and will be responsible for producing high-quality documentation for the international pharmaceutical industry.

Job OverviewWe are seeking a skilled Medical Writer to join our team for a 3-month period. This individual will be responsible for translating complex scientific and clinical information into clear and concise documents.The ideal candidate will have expertise in the healthcare and pharmaceutical industries, with a strong background in medical writing and...

Medical Content Translator and Writer Job DescriptionWe are looking for a Medical Writer with expertise in healthcare and pharmaceutical industries to join our team. The ideal candidate will be able to translate complex scientific and clinical information into clear and concise documents.Key Responsibilities:Clinical Writing: Prepare and edit clinical study...

Job Description: We are looking for a highly skilled CMC Regulatory Documentation Expert to join our team at RBW Consulting. In this role, you will be responsible for preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets.Responsibilities:- Prepare,...

Evaluate Your SkillsThis is your chance to take your career to the next level by joining our client's EMEA regulatory team in London.The ideal candidate will have a strong background in regulatory affairs, with experience in managing label development and compliance for flavor extensions and label change projects. You will also be responsible for...

Job OverviewPE Global requires a seasoned Pharma Regulatory Documentation Expert to spearhead Regulatory Records Management efforts in compliance with global regulations and industry standards.DutiesImplement comprehensive Regulatory Records Management solutions in tandem with RA Ops Mergers and Acquisitions Team.Establish effective communication channels to...