Regulatory Documentation Expert

Role OverviewA challenging opportunity has arisen for a Regulatory Affairs Strategist to join VRS Regulatory's team. About the RoleWe are seeking an experienced Regulatory Affairs Strategist to develop and implement regulatory strategies for plant protection products in specific geographical territories. Develop and execute regulatory strategies for product...

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,...

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...

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,...

As a Senior Regulatory Compliance Expert at Vixio Regulatory Intelligence, you will play a key role in shaping our company's technical compliance solution for online gaming operators and suppliers. This exciting opportunity allows you to leverage your expertise in regulatory requirements to design and develop a premium quality intelligence solution that...

Job OverviewA Document Writer at Emagine Consulting plays a crucial role in creating comprehensive documents for regulatory submission, summarizing compliance requirements. This dynamic individual will collaborate with subject matter experts to document processes and actions taken to meet regulatory frameworks such as MiFID, Basel III, FRTB, and more.The...

**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...

About the RoleThis is a unique opportunity to leverage your expertise in Regulatory Affairs (RA) and take on the responsibility of creating, reviewing, and updating procedural documents for RA owned processes.Key ResponsibilitiesDevelop clear, concise, and accurate RA owned procedural documents in alignment with respective functions.Collaborate with subject...

Established chemical regulatory science consultancy is seeking a delivery-focused Regulatory Affairs Specialist to cover an increasing workload.This role will take the lead on physical/chemical properties/analytical methods and method validation for plant protection products. Key responsibilities include:Providing clients with regulatory advice on substance...

**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 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...

Compliance ProfessionalsWe are a reputable broker and market maker in the financial services industry, focusing on futures, options, and other derivatives.We seek a highly detail-oriented Derivatives Documentation Expert to join our team.Key ResponsibilitiesDevelop and maintain comprehensive policy and procedure documentation to ensure compliance with...

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...

We 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...

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 DescriptionAs a Regulatory Affairs Manager at Prinova Europe, you will oversee regulatory strategy for the organisation, providing leadership and guidance to the business on regulatory matters for food, feed and personal care activity in the UK and other markets where Prinova Europe and Prinova Solutions Europe operates.This role involves ensuring...

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...

Park Street People is currently looking for a skilled Regulatory Affairs Expert to join their team in Cambridge or West London (Uxbridge). As a global pharmaceutical company, they have created a centre of excellence and constantly focus on driving innovation and using cutting-edge techniques in their science. The role is remote-by-design, but occasional...

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...