Clinical Documentation 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...

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...

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 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...

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...

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.

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...

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...

Company OverviewWorldwide Clinical Trials is a global team of over 3,500+ experts, bright thinkers, and doers dedicated to changing the way the world experiences CROs.Salary: The estimated salary for this role is $85,000 - $110,000 per year, depending on experience.Job DescriptionWe are seeking a highly motivated Regulatory Affairs Specialist to join our...

Job SummaryWe are looking for an experienced Operating Theatre Nurse Specialist to join our clinical team. As a key member of the ophthalmic theatre team, you will be responsible for providing high-quality patient care and contributing to the smooth operation of the theatre.Key responsibilities include providing direction and leadership to junior staff,...

Job OverviewThe Clinical Research Specialist will be responsible for the coordination and management of a clinical research portfolio, comprising in-house, national, and international phase I, II, and III clinical trials. This role will involve working within the multidisciplinary team to develop specialized skills and knowledge relating to the conduct of...

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...

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,...