Clinical Document Specialist

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...

Medical Writer Opportunity in Rare DiseasesHays Specialist Recruitment Limited is seeking a skilled Medical Writer to join their team for a 6-month contract in the rare diseases arena. As a Regulatory/Clinical Medical Writer, you will be responsible for creating high-quality regulatory and clinical documents, including protocols, core dossiers, CSRs, and...

At 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...

We 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...

Job 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...

A leading pharmaceutical organisation is seeking a Medical Document Reviewer to join their medical affairs team.Key Responsibilities:Review and approve documents from various teams, including customer support, marketing, regulatory, clinical, scientific, and medical.Collaborate with the AQP for medical affairs teams to ensure seamless document approval...

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...

Job Summary:Clinical Professionals Limited seeks a skilled Clinical Specialist to drive product advocacy and pathways across the territory.Key Responsibilities:Liaise with NHS stakeholders, HCPs, KOLs, and advocates to promote product adoption.Collaborate with established brands in Consumer and Clinical settings.Travel to the North of England and occasional...

Job Title: Clinical Evaluation Report SpecialistJob Summary: We are seeking an experienced Clinical Evaluation Report Specialist to join our Editorial team at Clinical Professionals Limited. The successful candidate will be responsible for creating high-quality scientific content for different audiences.Key Responsibilities:Develop and maintain a deep...

Job DescriptionThis role involves providing quality control review of clinical documents intended for submission to health authorities worldwide. The Senior Medical Editor will copyedit/proofread, format, and verify data content in clinical documents in accordance with SOPs and processes to ensure documents meet required standards.Responsibilities:Perform QC...

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 George ClinicalGeorge Clinical is a leading global clinical research organization that has been driving scientific excellence and operational efficiency for over 20 years.With a strong presence in the Asia-Pacific region, USA, and Europe, we offer a full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers.Our...

Worldwide Clinical Trials, a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company's scientific heritage, we develop flexible plans and solve problems quickly for our customers...

Job Title: Associate Director of Medical WritingJob Overview:Clinical Professionals Limited is seeking an experienced Associate Director of Medical Writing to lead our medical writing activities and serve as an expert Medical Writer. The successful candidate will be responsible for planning, developing, and writing clinical and regulatory documents to...

Clinical Professionals Limited is seeking a Clinical Advocacy Specialist to join their team in the North of England. This role involves working with NHS stakeholders, HCPs, KOLs, and advocates across the territory to drive product advocacy, pathways, and prescription initiations.About the RoleThe primary aim of this role is to utilise your clinical knowledge...

We are seeking an experienced Freelance Regulatory Medical Writer to join our team at Empatico Consulting. This is a unique opportunity to work with a fast-growing biotech company that discovers and develops immunotherapeutic products and vaccines for the treatment and prevention of infectious diseases and cancer.As a Freelance Regulatory Medical Writer, you...

We are seeking a professional and experienced Autism Diagnostic Observation Schedule (ADOS) specialist to join our team at Clinical Partners Ltd, conducting face-to-face assessments for both children and adults in Merseyside, Knowsley, and Leeds.This is a unique opportunity to play a key role in the diagnostic process, helping to identify autism spectrum...

Are you a skilled medical writer looking for a new challenge? We are seeking an experienced MEDICAL WRITER SPECIALIST to join our team at Worldwide Clinical Trials, a leading global contract research organization.We offer a competitive salary of €80,000 - €110,000 per year, depending on experience, plus benefits and opportunities for professional...

Job SummaryWe are seeking an experienced Commercial Contract Specialist to join our team at Clinical Professionals Limited. This role will involve drafting and negotiating commercial contracts, providing legal support and advice, and maintaining a comprehensive understanding of contract law and regulations.

OverviewAt Pharmaceutical Research Associates, Inc, we are seeking a highly skilled Clinical Trial Transparency Specialist to join our team. As a Clinical Trial Transparency Specialist, you will be responsible for supporting the client's clinical trial transparency processes in compliance with trial transparency laws and requirements and client...