Clinical Development Document Specialist

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...

Job 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...

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...

Job 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...

MMS Holdings Inc. is a leading Contract Research Organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with innovative data-focused services.Job SummaryWe are seeking a highly experienced Clinical Development Specialist to join our team. In this role, you will be responsible for critically evaluating medical literature,...

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...

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...

MMS 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.Key ResponsibilitiesCritical Evaluation and Analysis: The Medical Writer will critically evaluate, analyze, and interpret the medical...

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 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...

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...

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...

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...

Job Title: Clinical Service Development LeadWe are seeking a talented Clinical Service Development Lead to join our team at First Clinical Ltd. As a clinically qualified and experienced healthcare professional, you will play a crucial role in developing and implementing new clinical services and improving existing ones.About the Role:Development of new...

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...

At Worldwide Clinical Trials, we are a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to advance new medications from discovery to reality.We offer a competitive salary of $120,000 - $180,000 per annum, based on experience, as well as a range of benefits including health...

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...