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Kaufmännische Tätigkeiten » Regulatory Affairs & Management

Regulatory Documentation Writer Stellenangebote

Ihre Jobsuche nach Regulatory Documentation Writer Jobs ergab 14 Stellenangebote

Stellenangebote Regulatory Documentation 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 [...] of all clinical and submission documentation across all aspects of the compounds life cycle management. Due to the complexity of the programs, the incumbent must rapidly [...] Global Investigator Brochures, and annual regulatory reports Leads the medical writing activities for marketing application submission documents Liaises with other functional areas and groups in the [...]
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Stellenangebote Regulatory Documentation 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 [...] of all clinical and submission documentation across all aspects of the compounds life cycle management. Due to the complexity of the programs, the incumbent must rapidly [...] Global Investigator Brochures, and annual regulatory reports Leads the medical writing activities for marketing application submission documents Liaises with other functional areas and groups in the [...]

Stellenangebote Regulatory Documentation Writer Jobs bei Freelance.de

Job vor 8 Tagen gefunden

Für Freelancer- Technical Writer (f/m/d)

• Zug Freelancer Projekt- Technical Writer (f/m/d) - Frame Maker/ Ixiasoft/ ST4/ German/ international Project: For our customer Roche Diagnostics International AG based in Rotkreuz we [...] while respecting project timelines and documentation standards, guidelines, and templates. Independently gathers and consolidates the information needed for the technical content creation. Creates content. Works closely [...] that quality targets, timelines, and regulatory requirements are respected. After translation, creates target language versions of deliverables (in all appropriate formats) . Uses knowledge and expertise [...]

Weitere Stellenangebote Regulatory Documentation Writer bei Jobleads

Job vom 29.03.2024

Medical Writer I

• München, Bayern [...] Project and have experience with documentation systems. The applicant must have experience in leading and facilitating teams to finalize reports with approvals per standard operating procedures. [...] pharmaceutical development processes, cGMPs and regulatory requirements are required. Excellent English, writing and oral presentation skills is mandatory Prior experience with Pharmaceutical Industry is mandatory Prior [...] years experience as a Technical Writer 2+ years primary role writing user documentation for a variety of products, prepared as part of an integrated team [...]

Job vom 29.03.2024

Medical Writer I, II or III

• München, Bayern [...] 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 implementation of the [...] formats and guidelines for clinical documentation. May prepare scientific manuscripts, abstracts and posters. May also support clinical research associates and medical doctors in clinical protocol development. [...]
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Job vom 29.03.2024

Contract Medical Writer

• München, Bayern [...] 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 delivery of final drafts for regulatory fulfilment of assigned therapeutic areas and/ or products in Clinical Development to US and other global health authorities using appropriate [...] concisely prepare all clinical regulatory documentation, including major submission and/ or complex documents in English. Excellent understanding of biostatistics reporting standards and awareness of the associated [...]

Stellenangebote Regulatory Documentation Writer Jobs bei NewScientist Jobs

Job vor 4 Tagen gefunden

Sr Clinical Research Scientist (Hybrid)

• Cambridge, Massachusetts, Cambridge Aequor Technologies LLC [...] study teams, ethics committees or regulatory authorities, help manage study committees. Scope includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vor 4 Tagen gefunden

USA- Scientist III (Scientific)

• Cambridge, Massachusetts, Cambridge Talent Burst, Inc. [...] study teams, ethics committees or regulatory authorities, help manage study committees. Scope includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vor 4 Tagen gefunden USA- Scientist III (Scientific) • Cambridge, Massachusetts, Cambridge Hire Talent [...] study teams, ethics committees or regulatory authorities, help manage study committees. Scope includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vor 4 Tagen gefunden USA- Scientist III (Scientific) • Cambridge, Massachusetts, Cambridge eTeam Inc. [...] study teams, ethics committees or regulatory authorities, help manage study committees. Scope includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vor 4 Tagen gefunden USA- Scientist III (Scientific) • Cambridge, Massachusetts, Cambridge Mindlance [...] study teams, ethics committees or regulatory authorities, help manage study committees. Scope includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vor 4 Tagen gefunden Scientist III • Cambridge, Massachusetts, Cambridge Integrated Resources, Inc [...] study teams, ethics committees or regulatory authorities, help manage study committees. Product includes all R D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy) [...] 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 ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. To [...]

Job vom 12.04.2024 Technical Operations Lead • United States Charles River [...] review, and approve GMP technical documentation for the Right Source group and advisementor the group on best practices. Manage GMP operational workflows at the site or [...] years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of [...] Pharmaceutical, Operations Manager, Laboratory, Technical Writer, Science, Operations, Technology 74703189 [...]

Job vom 04.04.2024 Training Specialist Lead • Memphis, Tennessee, United States, Memphis Charles River [...] certifications Modify and revise training documentation and programs as needed Provide effective training materials utilizing a variety of media Coach others involved in training efforts, providing [...] years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of [...] Segment: Pharmaceutical, Laboratory, Training, Technical Writer, Document Management, Science, Operations, Technology 72010783 [...]

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