Regulatory Document Writer

Job Title: Senior/Principal Medical WriterCompany: Trilogy Writing & ConsultingWe are seeking a highly skilled Senior/Principal Medical Writer to join our team at Trilogy Writing & Consulting. As a Senior/Principal Medical Writer, you will be responsible for preparing clinical regulatory documents, including Clinical Study Protocols, Clinical Study Reports,...

About the RoleWe are seeking a Senior/Principal Medical Writer to join our team at Trilogy Writing & Consulting. As a Senior/Principal Medical Writer, you will be responsible for preparing clinical regulatory documents, including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures. You will work collaboratively with client authoring...

Job Title: Principal Medical WriterWe are seeking a highly skilled Principal Medical Writer to join our IAI Medical Writing Team at Syneos Health. As a key member of our team, you will be responsible for developing clinical documents for submissions to regulatory authorities globally.Key Responsibilities:Develop scientifically valid, complete, and consistent...

Job Title: Corporate Writer for External ReportingWe are seeking a seasoned writer to join our team at MatchaTalent. The ideal candidate will have a strong background in writing, editing, and proofreading, with experience in creating high-quality reports for external stakeholders.About the Role:Write and edit material for publication in our Annual and...

Job Title: Medical Writing Manager - Oncology RegulatoryJob Summary:We are seeking a highly skilled Medical Writing Manager to join our Oncology Regulatory team at Johnson & Johnson Innovative Medicine. As a Medical Writing Manager, you will be responsible for leading a team of medical writers in the preparation and finalization of clinical documents.Key...

Medical Writer - Regulatory AffairsMMS Holdings Inc is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.As a Medical Writer - Regulatory Affairs, you will be responsible for critically...

Regulatory Documentation Specialist RoleTrilogy Writing & Consulting, an Indegene Company, is currently seeking a highly skilled Regulatory Documentation Specialist to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry.As a key member of our team, you will be integral to the writing...

Job Title: Clinical Document DeveloperPharmiweb is seeking a skilled Clinical Document Developer to join our team. As a key member of our Medical Writing team, you will be responsible for developing high-quality clinical documents for regulatory submissions.Key Responsibilities:Develop clinical study protocols and amendments, clinical study reports (CSRs),...

Job SummaryWe are seeking a highly skilled Senior Clinical Document Developer to join our team at Syneos Health. As a key member of our IAI Medical Writing Team, you will be responsible for developing clinical documents for submissions to regulatory authorities globally.Key ResponsibilitiesDevelop scientifically valid, complete, and consistent clinical...

Job DescriptionGlobal Pharmacovigilance Safety Coordinator OpportunityMain ActivitiesDocument Preparation: Schedule and maintenance of the planning of all safety reports for medicinal products and medical devices across different geographies where Angelini is present.Ensure proper coordination of safety reports preparation/submission/maintenance working in a...

MMS Holdings Inc. is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.We are seeking a highly skilled Regulatory Medical Writer to join our team.Responsibilities:Under minimal supervision, the...

Job Role: Regulatory Affairs CMC SpecialistWe are looking for a highly skilled Regulatory Affairs CMC Specialist to join our team at EUSA Pharma. The ideal candidate will have consolidated experience on Chemistry, Manufacturing, and Control (CMC) aspects in order to manage the preparation of dossiers for submission to regulatory authorities worldwide.Key...

MMS Holdings Inc. is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.We are seeking a highly skilled and experienced Regulatory Document Specialist to join our team.Responsibilities:Under...

About the RoleMMS Holdings Inc is seeking a dedicated and experienced Medical Writing Consultant to join our team. As a key member of our clinical operations team, you will be responsible for creating high-quality clinical documents, including clinical protocols, investigator's brochures, and clinical study reports.Key ResponsibilitiesEvaluate and analyze...

MMS Holdings Inc. is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.We are seeking a highly skilled Medical Writer to join our team. The ideal candidate will have a strong background in...

Job Title: Senior Medical Writing ConsultantAbout Us: MMS Holdings Inc is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. We have a global footprint across four continents and maintain a 97 percent customer...

About Mms Holdings IncMms Holdings Inc is a leading Contract Research Organization (CRO) that provides innovative, data-focused solutions to the pharmaceutical, biotech, and medical device industries.Job DescriptionWe are seeking a highly skilled Medical Writer to join our team. As a Medical Writer, you will be responsible for critically evaluating,...

About MMS Holdings Inc.MMS Holdings Inc. is a leading Contract Research Organization (CRO) that provides innovative, data-focused solutions to the pharmaceutical, biotech, and medical device industries. With a proven scientific approach to complex trial data and regulatory submission challenges, MMS supports clients in creating compelling submissions that...

Job Title: Senior Medical Writing ConsultantAbout the Role:MMS is an innovative, data-focused CRO that supports 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...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Safety Specialist to join our team at Angelini Pharma. The successful candidate will be responsible for coordinating the preparation and submission of safety reports for medicinal products and medical devices across various geographies.Main ResponsibilitiesDocument Preparation: Schedule and...