Clinical Research Writer Stellenangebote
Ihre Jobsuche nach Clinical Research Writer Jobs ergab 19 Stellenangebote
Stellenangebote Clinical Research Writer Jobs bei Jobleads
Job vom 30.03.2024
Associate Director, Medical Writing- Neuroscience
• München, Bayern
[...] be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/ contractors on [...] accuracy and quality of all clinical and submission documentation across all aspects of the compounds life cycle management. Due to the complexity of the programs, the [...] structure Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program Implements document quality controls, [...]
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Stellenangebote Clinical Research Writer Jobs bei Stellen-Online.de
Job vom 31.03.2024
Associate Director, Medical Writing- Neuroscience
• München, 80333
Integrated Resources Inc.
[...] be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/ contractors on [...] accuracy and quality of all clinical and submission documentation across all aspects of the compounds life cycle management. Due to the complexity of the programs, the [...] structure Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program Implements document quality controls, [...]
Weitere Stellenangebote Clinical Research Writer bei Jobleads
Job vom 30.03.2024
Medical Writer- I
• München, Bayern
[...] areas: Information Technology (IT) , Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client Job Description Overview: The Medical Writer Specialist is responsible for preparation of documents that support the presentation and/ or publication needs of assigned therapeutic areas and/ [...]
Job vom 30.03.2024
Medical Writer Position
• München, Bayern
[...] areas: Information Technology (IT) , Clinical Research, Rehabilitation Therapy and Nursing. Job Description RESPONSIBILITIES: Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory [...]
Job vom 29.03.2024
Medical Writer I, II or III
• München, Bayern
[...] Corporation (MTPC) , is a research- driven pharmaceutical company with global reach and one of Japan s oldest and most respected companies. Relatively new to the [...] a key member of our Clinical Development Team, the Medical Writer will provide regulatory documents support to the clinical teams, ensuring successful preparation of high quality, submission- ready documents and effective [...]
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Job vom 29.03.2024
Senior Medical Writer (Home Based)
• München, Bayern
[...] and commercialize drugs. At INC Research/ inVentiv Health our 22, 000 employees have one purpose: shortening the distance from lab to life. You ll work alongside [...] Serves as a senior medical writer on clinical study or regulatory project teams. Plans and coordinates report- writing activities with dependent staff roles to ensure satisfactory completion of [...]
Job vom 29.03.2024
Medical Writer III : 4710313
• München, Bayern
[...] develop and/ or edit scientific/ clinical documents, including manuscripts, abstracts, posters, and slide presentations Work effectively with company document management systems and related tools, templates, and [...] 10 years) as a medical writer or equivalent working knowledge of clinical research, study design, and ability to present clinical data objectively in a clear, concise written format Demonstrated competency in project management [...]
Job vom 29.03.2024
Medical Writer V
• München, Bayern
[...] for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance [...]
Job vom 29.03.2024
Contract Medical Writer
• München, Bayern
[...] for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance [...] partners. Job Description Contract Medical Writer Remote Job Description The Contract Medical Writer authors, edits and provides high- quality clinical documents from planning and coordination through [...]
Job vom 29.03.2024
Senior medical writer
• München, Bayern
[...] for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance [...]
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Stellenangebote Clinical Research Writer Jobs bei NewScientist Jobs
Job vor 3 Tagen gefunden
Sr Clinical Research Scientist (Hybrid)
• Cambridge, Massachusetts, Cambridge
Aequor Technologies LLC
[...] help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vor 3 Tagen gefunden
USA- Scientist III (Scientific)
• Cambridge, Massachusetts, Cambridge
Hire Talent
[...] help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vor 3 Tagen gefunden
USA- Scientist III (Scientific)
• Cambridge, Massachusetts, Cambridge
Talent Burst, Inc.
Industry: Biotechnology Position: Clinical Scientist III Location: Cambridge, MA (Hybrid: 2/ 3 days per week remote) Duration: 12 months contract (+Possibility of extension) Details: [...] of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vor 3 Tagen gefunden
USA- Scientist III (Scientific)
• Cambridge, Massachusetts, Cambridge
eTeam Inc.
[...] join a team supporting a clinical program with one phase 2 trial, two core phase 3 and a phase 3 LTS trial (in total, 100 sites [...] of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vor 3 Tagen gefunden
Scientist III
• Cambridge, Massachusetts, Cambridge
Integrated Resources, Inc
[...] help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vor 3 Tagen gefunden
USA- Scientist III (Scientific)
• Cambridge, Massachusetts, Cambridge
Mindlance
[...] help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical Sciences Operations Platform (CSO) [...] Feasibility Managers, Pharmacovigilance representative, Medical Writer (e. g. planning and review of narratives) on high quality medical review, as needed. He/ she supports the CRD to [...]
Job vom 12.04.2024
Technical Operations Lead
• United States
Charles River
[...] years related technical experience in research or pharmaceutical environment. Must have a background in cGMP operations required. An equivalent combination of education and experience may be [...] cell banks through preclinical and clinical studies to marketed products. Whether clients need stand- alone services, a unique package of testing, or insourced support, our Biologics [...] Pharmaceutical, Operations Manager, Laboratory, Technical Writer, Science, Operations, Technology 74703189 [...]
Job vom 10.04.2024
QC Specialist III Microbiology
• Memphis, Tennessee, United States, Memphis
Charles River
[...] cell banks through preclinical and clinical studies to marketed products. Whether clients need stand- alone services, a unique package of testing, or insourced support, our Biologics [...] is an early- stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio [...] Job Segment: Pharmaceutical, Laboratory, Technical Writer, Statistics, CAPA, Science, Technology, Data, Management 74386280 [...]
Job vom 04.04.2024
Training Specialist Lead
• Memphis, Tennessee, United States, Memphis
Charles River
[...] based document management systems in clinical and commercial pharmaceutical/ biopharmaceutical manufacturing Excellent working knowledge and experience with the practical implementation of FDA and EMA regulations and [...] is an early- stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio [...] Segment: Pharmaceutical, Laboratory, Training, Technical Writer, Document Management, Science, Operations, Technology 72010783 [...]
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