7 clinical report writer jobs at 6 companies in United States
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Clinical Evaluation Report (CER) Writer
United States
RemoteMultiple Commitments Available
1+ YOEBA/BS in science/engineering/medical field,1+ years medical writing experience (device industry preferred),EMB/Word/Excel proficiency,knowledge of EU device regulations,and ability to perform literature reviews and database searches.
Microsoft Office 365, Word, Excel, Teams, Outlook, SharePoint, EndNote, QUOSA, Distiller, FDA MAUDE, FDA Recall Database
2mo
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Principal Medical Writer
Durham or London
OnsiteFull Time
5+ YOEBachelor's in life/health sciences, 5+ years medical or regulatory writing in pharma/healthcare, 3+ years regulatory dossier/CTD experience, 3+ years authoring protocols and clinical study reports.
2mo
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Principal Medical Writer
Durham or London
OnsiteFull Time
5+ YOEBachelor's in life/health/scientific field, 5+ years medical or regulatory writing in pharma, 3+ years regulatory dossier and CTD experience, 3+ years independently authoring protocols and clinical study reports; strong writing, teamwork, and regulatory knowledge.
Common Technical Document (CTD), International Council for Harmonisation (ICH), Good Clinical Practice (GCP)
1mo
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Principal Medical Writer - Publications
Pennsylvania, United States
$81k-$176k/yr RemoteFull Time
Proven experience leading complex medical writing for regulatory and scientific documents (e.g., clinical study reports, protocols, NDA/eCTD submissions), familiarity with ICH E3 and regulatory standards, strong scientific judgment, mentoring experience, and ability to manage timelines and budgets.
2mo
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Clinical Systems Analyst - 2
Stamford, Connecticut, United States
OnsiteFull Time, Temporary
10+ YOEBachelor's degree required (Masters preferred); 10+ years managing/directing technology/security operations (healthcare preferred); experience with HIS applications, Meditech report writer; NIST Framework preferred; project and vendor coordination skills.
Meditech Non-Procedural Representation Report Writer, Meditech, NIST Framework
5d
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Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK
United States or Canada or United Kingdom
$81k-$176k/yr RemoteFull Time
5+ YOERequires 5+ years of lead regulatory writing experience, Phase 2 and 3 experience, expertise with clinical protocols, submissions, CSRs, IBs, safety reports, strong project management, client, and time management skills.
ICH E3, FDA, EMA, CTD, eCTD
1mo
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Advanced Practice Provider (Nurse Practitioner or Physician Assistant)
Covington, Louisiana, United States
OnsiteFull Time
3+ YOELicensed NP or PA in Louisiana with national certification and DEA registration if applicable; MSN/DNP or Master\u0002s for PA; minimum 3 years APP experience preferred; proficiency with Microsoft Office and Crystal Report Writer; strong clinical oncology and surgical breast knowledge.
Microsoft Office, Crystal Report Writer