Clinical Writer Stellenangebote


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17 Stellenangebote


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Job vom 11.10.2024

Lead Medical Writer (Reporting to Vice President Regulatory Affairs)

• Wuppertal, Nordrhein- Westfalen Führungs-/ Leitungspositionen
MEHRYour mission As a Lead Medical Writer, you will plan, author, and organize the review process of documents pertaining to clinical studies and regulatory interactions, including (but not limited to) critical sections of marketing applications, protocols, clinical study reports, briefing documents, [...]
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Jobbörse Stellenangebote Clinical Writer Jobs gefunden bei Jobbörse StepStone

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Stellenangebot Clinical Writer Job bei JOTEC GmbH Job vom 17.08.2024 JOTEC GmbH

Head of Medical Writing (m/f/d)

• Hechingen Führungs-/ Leitungspositionen Homeoffice möglich
MEHR[...] hiring HEAD OF MEDICAL WRITING m/f/d Establish medical and regulatory writing best practices (templates, SOPs, work instructions, document review, document timelines) to ensure consistency and quality of documents Lead writing team to ensure the generation of key documents in internal clinical partnerships with relevant functions (Project Management, Data Management and CRAs) on schedule and the support of key documents in Artivion [...] preparation for document reviews in an efficient manner Oversight of medical and regulatory writing vendors in alignment with global internal resources, methods, SOPs, and overall approach Degree in medicine or natural science Long- standing years of experience as a medical writer in the medical/ biomedical industry with evidence of increasing responsibility and technical development Proficient at writing protocols, manuscripts and study [...]
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Job vor 8 Tagen gefunden

Director, Regulatory Medical Writing (1 of 4)

Führungs-/ Leitungspositionen
MEHR[...] This is a global role and is open to other countries. Remote work options may be considered on a case- by- case basis and if approved by the company. The Director, Regulatory Medical Writing (RegMW) is a highly experienced medical writer and influential leader with strategic responsibilities as it relates to the delivery of high- quality regulatory documentation. This position will [...] strategist is the primary RegMW interface to the Compound Development Teams (CDTs) at the early stages of submission preparation and the RegMW expert for the delivery of Johnson Johnson Innovative Medicine marketing applications. Principal Responsibilities: Leadership: With a focus on clinical scientific content, lead early strategic submission discussions in collaboration with Key Stakeholders and Senior Leadership that are grounded in Label [...]
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Jobbörse Stellenangebote Clinical Writer Jobs gefunden bei Jobbörse jobDENTAL

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Job vom 28.09.2024 Geistlich Biomaterials Vertriebsgesellschaft mbH

Clinical Science Education Manager (m/w/d) in Baden Baden

• 76534 Baden- Baden Homeoffice möglich Firmenwagen Flexible Arbeitszeiten
MEHREinleitung Zur Verstärkung unseres Geistlich- Teams suchen wir Sie schnellstmöglich als Clinical Science Education Manager (m/w/d) Baden- Baden, Vollzeit Wir bieten Ihnen Attraktives Gehaltspaket Flexible Arbeitszeiten, Homeoffice Dienstwagen Betriebliche Krankenzusatzversicherung Altersvorsorge Kostenloser [...] (EU Rep) Sie sind Teil des lokalen Leadershipteams Ihr Profil Universitätsabschluss mit einem naturwissenschaftlichen oder zahnmedizinischen Hintergrund Sie haben mind. 1- 2 Jahre Berufserfahrung im Vertrieb, Marketing, Regulatory oder in der klinischen Wissenschaft im Gesundheitswesen (Scientific Affairs, Medical Affairs, Scientific writer) Sie sind ein Teamplayer und schätzen die abteilungsübergreifende, interdisziplinäre Zusammenarbeit Sie Überzeugen durch Verbindlichkeit und Auftreten und können komplexe Themen [...]
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Jobbörse Stellenangebote Clinical Writer Jobs gefunden bei Jobbörse NewScientist Jobs

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Job vor 6 Tagen gefunden Calyx

Medical Writer I

• Hammersmith, London, United Kingdom, London (Greater)
MEHR[...] buy more) HEALTH Private Healthcare Optional dental insurance, health assessments and health cash plans Cycle to Work scheme WEALTH Company Pension Scheme, matching contributions up to 5 of salary Life assurance Annual staff bonus scheme Season ticket loans The Medical Writer I plays a critical role in the development, editing, and finalization of study- specific documents, a number of which may [...] create efficiencies in document authoring. Oversees and coordinates document development for assigned projects. Education: Master s degree in Life Sciences/ Health Related Sciences or equivalent experience. Experience: 3 years of experience writing scientific, medical, or technical content, preferably in a clinical research setting Demonstrated understanding of clinical research, the drug development process, and applicable regulatory guidelines Qualifications: Strong communication skills Excellent [...]
Job vor 6 Tagen gefunden Bio Marin Pharmaceutical Inc.

Associate Medical Director, Clinical Science

• London, Greater London, United Kingdom, London (Greater) Führungs-/ Leitungspositionen
MEHR[...] the right technical expertise and a relentless drive to solve real problems- and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well- understood biology and provide an opportunity to be first- to- market or offer a [...] review, review of blinded tables, listings and figures (TLFs) , etc. ) and actively participate in all data snapshots taken (not limited to final DBL) Contribute to and review Clinical Study Report (CSR) writing (review final TLFs, work with medical writer to review revise CSR document, draft discussion and conclusions, participate in comment resolution meetings) Present study updates and topline results [...]
Job vor 10 Tagen gefunden Richmond Pharmacology

Medical Writer

• London, United Kingdom, London (Greater)
MEHRJob Title: Medical Writer Location: On- Site (London Bridge) Term: Permanent, Full- time Salary: Competitive + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays Many more) Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early- phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and [...]
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Job vom 01.11.2024 Fortrea

Medical Writer 1

• Leeds, United Kingdom, West Yorkshire
MEHRAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology [...] areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Do you have a passion for scientific writing and clinical research? Then, join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick- starting a global career in clinical trials. As [...]
Job vom 01.11.2024 Fortrea

Principal Medical Writer sponsor dedicated

• Maidenhead, United Kingdom, Berkshire
MEHRAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology [...] the globe. Full time. Remote. UK, France, Spain or Portugal. We are on a mission to deliver solutions that bring life- changing treatments to patients faster. But we can t do it alone. We are seeking an experienced Principal Medical Writer to lead authoring and development of high complexity clinical regulatory documents that are critical to the strategic projects of our [...]
Job vom 27.10.2024 Rx Logix Corporation

Content Writer- Pharmacovigilance

• London, United Kingdom, London (Greater)
MEHR[...] s PV Surveillance Suite Platform to replace its legacy FAERS signaling system, utilizing our modules for advanced data analytics, signal detection, evaluation, signal management, and benefit- risk assessment. Job Description: We re on the hunt for a dynamic, creative Content Writer with a solid background in pharmacovigilance. This role calls for a strategic thinker who can understand our product offerings and [...] practices in all content development activities. Scientific and Technical Writing: Proficiency in medical terminology and scientific writing. Excellent writing skills with attention to detail and accuracy. Competence in reviewing and editing pharmacovigilance documents. Research and Data Analysis: Ability to interpret clinical trial data and scientific literature. Skill in conducting literature searches and critically evaluating scientific literature. Familiarity with pharmacovigilance databases and [...]
Job vom 26.10.2024 Richmond Pharmacology Principal Medical Writer • London, United Kingdom, London (Greater)
MEHRJob Title: Principal Medical Writer Location: London Bridge (Hybrid 4 Days onsite) Term: Permanent, Full- time Salary: Competitive Salary + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays Many more) Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early- phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and [...]
Job vom 13.10.2024 Bio Marin Pharmaceutical Inc. Associate Director, Clinical Medical Writing • London, Greater London, United Kingdom, London (Greater) Führungs-/ Leitungspositionen
MEHR[...] the right technical expertise and a relentless drive to solve real problems- and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well- understood biology and provide an opportunity to be first- to- market or offer a [...] consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. EDUCATION REQUIREMENTS Masters (MS) or higher degree preferred; scientific focus desirable. Minimum requirement: At least 10- years of experience as a medical writer in the pharmaceutical industry. Evidence of medical writing career development desirable, e. g. European/ American Medical Writers Association certificate, Editor [...]
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Job vom 12.10.2024 MMS Principal Medical Writer- Remote • London, United Kingdom, London (Greater)
MEHRMMS is an innovative, data- focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong [...] has been recognized as a leading CRO in Global Health Pharma s international awards programs for the last three consecutive years. For more information, visit www. mmsholdings. com or follow MMS on Linked In. Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, [...]
Job vom 12.10.2024 MMS Senior Medical Writer (Remote) • London, United Kingdom, London (Greater)
MEHR[...] has been recognized as a leading CRO in Global Health Pharma s international awards programs for the last three consecutive years. For more information, visit www. mmsholdings. com or follow MMS on Linked In. Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias Write and edit clinical development documents, including but not limited to, clinical protocols, investigator s brochures, clinical study reports, subject consent forms, integrated safety [...]
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