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Entry level medical writer Jobs in Minneapolis, MN
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Nonclinical Medical Writer
VirtualVocationsSaint Paul, Minnesota, United States- Promoted
Associate Quality Engineer - Medical Device (Entry / Junior Level)
Planet PharmaMinneapolis, MN, United States- Promoted
Entry Level Microbiologist
Pace Analytical Services, LLCSt Paul, MN, United StatesCustoms Entry Writer
Kuehne+NagelMinneapolis / St Paul Apt, MN, USEntry-Level Investigator
Ethos Risk ServicesMinneapolis, MN, USA- Promoted
Entry Level Microbiologist
Pace Life SciencesSt Paul, MN, United States- Promoted
Maintenance Technician (Entry Level)
Yellow TreeSaint Paul, MN, US- Promoted
- New!
Welder (ENTRY LEVEL)
AerotekSaint Paul, MN, US- Promoted
Account Manager Entry Level
Gypsum ConsultingMinneapolis, MN, United States- Promoted
Scheduling Coordinator (Entry-Level)
Katapult NetworkMinneapolis, MN, USCanvasser (Entry Level)
Revel PaintingMinneapolis, MN, US- Promoted
Hvac Technician - Entry Level
AEROTEKSaint Paul, MN, USEntry Level Manager
Paradox MarketingNorth Loop, MN, US- Promoted
Medical Assistant - Entry Level Training Program
Dreambound Inc.Minneapolis, Minnesota- Promoted
Entry Level Sales
Results ContractingMinneapolis, MN, US- Promoted
Entry Level Sales Representative
Total Quality LogisticsMinneapolis, MN, United States- Promoted
Telecommunication Technician Entry Level
LumenBROOKLYN CENTER, MN, United StatesMedical Writer / Editor
Taylor CorporationRemote, MN- Promoted
Account Manager - Entry Level
Scope Solutionssaint paul, MN, United States- Promoted
Warehouse Associate - Entry Level
Ferguson EnterprisesSt Paul, MN, United StatesNonclinical Medical Writer
VirtualVocationsSaint Paul, Minnesota, United States- Part-time
A company is looking for a Nonclinical Medical Writer (Part Time).Key ResponsibilitiesDevelop and manage nonclinical regulatory writing deliverables and documentationCoordinate and author nonclinical regulatory documents, ensuring integration of scientific and regulatory inputParticipate in IND or CTA subteams, managing timelines and document organizationRequired Qualifications7 years of experience in the research medical pharmaceutical or biotechnology industryMinimum of 5 years as a medical writer preparing regulated documents, particularly in oncology or rare diseasesTechnical expertise in Microsoft Office and Adobe Acrobat; familiarity with document management systemsGood understanding of global pharmaceutical drug development and regulatory submission requirementsBachelor's degree required; advanced degree preferred