Remote Principal Medical Editor — Regulatory Copy & QA Lead
Syneos Health, Inc.
- Remote job
Syneos Health seeks a Principal/Sr Medical Editor for Regulatory Documents, focused on copy editing, quality control, and ensuring regulatory documents meet sponsor and regulatory standards across FDA/EU guidelines. This role is NA/Canada remote-based. You will lead editorial activities on complex medical writing projects, mentor staff, and train editors while managing timelines and budgets. Strong AMA style familiarity is essential. #J-18808-Ljbffr Syneos Health, Inc.
- Syneos Health is seeking a Principal/Senior Medical Editor for Regulatory Documents, focusing on copy editing and QC, with remote work based in NA/Canada. You will join a global biopharmaceutical solutions leader, collaborating with medical writing, clinical development...Remote jobPrincipalRegulatory
$62k - $108.6k
Principal/Sr Medical Editor - Regulatory Documents - Copy Editing + QC - NA/Canada Remote Based Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and...Remote jobPrincipalRegulatoryContract workFlexible hours$62k - $108.6k
Syneos Health/ inVentiv Health Commercial LLC is seeking a Principal/Sr Medical Editor to ensure compliance with FDA and EU regulations. This remote role requires strong copy editing skills and the ability to mentor junior editors. The candidate will oversee timelines,...Remote jobPrincipalRegulatory$62k - $108.6k
Syneos Health/ inVentiv Health Commercial LLC is seeking a Principal/Sr Medical Editor for a remote role focusing on regulatory documents. This position involves a variety of responsibilities, including ensuring compliance with FDA and EU guidelines, managing timelines...Remote jobRegulatoryFlexible hours- Syneos Health, Inc. is seeking a Principal I/II Medical Writer (Clinical/Submissions) to join our fully remote team serving sponsors in Europe. The role focuses on end-to-end regulatory documentation for submissions and lifecycle management. The successful candidate will...Remote jobPrincipalRegulatory
- Veristat is seeking a Principal Medical Writer with CMC focus for remote work. You will lead authoring for complex regulatory submissions, mentor junior writers, and drive document quality across modules, including Module 3 and 2.3, ensuring alignment with global health...Remote jobPrincipalRegulatory
- BioMarin Pharmaceutical Inc. is seeking a Principal Clinical Medical Writer to lead the medical writing function within Development Sciences. The role... ...medical writing staff, manage timelines, and contribute to regulatory filings while collaborating with cross-functional...Remote jobPrincipalRegulatory
- Syneos Health, Inc. seeks a Senior/Principal Medical Writer with a regulatory focus to lead and manage medical writing deliverables across studies, ensuring accuracy... ...writers, and maintaining timelines within budget. Remote work is available in the US, UK, and Canada. The...Remote jobPrincipalRegulatory
- Leading the development of high-quality regulatory and clinical documents, the full-time Principal Medical Writer will oversee medical writing workstreams, collaborate with cross-functional... ...teams, and mentor junior writers in a remote setting. Key responsibilities Lead the...Remote workPrincipalRegulatoryFull time
- Veristat is seeking a Principal Medical Writer with a clinical focus to lead authoring and mentoring across regulatory documents for diverse client engagements. This fully remote role supports US, Canada, and international sites, and centers on delivering high-quality...Remote jobPrincipalRegulatory
- Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. The Principal Medical Writer will lead clinical documentation efforts and manage complex regulatory submissions. They will collaborate with cross...Remote jobPrincipalRegulatoryWorldwide
- ...Therapeutics is seeking an experienced Principal Medical Writer to independently author and oversee... ...will have strong scientific judgment, regulatory writing expertise, and the ability to... ...briefing documents etc.) Independently lead cross-departmental document development...Remote workPrincipalRegulatoryWork at officeFlexible hours
- Syneos Health, Inc. seeks a Sr. Principal Medical Writer to lead regulatory submission documents across global programs, including ICH-compliant materials (ISE/ISS/Clinical Overview). Remote role with major responsibilities for strategy, timelines, and cross-functional...Remote jobPrincipalRegulatory
- ...With deep domain expertise in regulatory sciences, clinical research... ...compliance, pharmacovigilance, medical information, and R&D... ...level documents) as assigned. Leads cross-functional coordination... ...Whilst ProPharma supports remote working, we also recognize the...Remote workPrincipalRegulatoryContract workWork at office
- ...ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with... ...Experience working in multicultural or remote team settings. Proven ability to...Remote workPrincipalRegulatoryLocal area
- Veristat is seeking a Principal Medical Writer to lead the authoring and mentoring of regulatory documents across multiple service lines. The PMW will serve as project leader, ensuring high-quality submissions and knowledge transfer within the team. Responsibilities include...Remote jobPrincipalRegulatory
$80.6k - $175.7k
...Principal Medical Writer - Publications Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We... ...scientific meetings. • Adheres to established regulatory standards, including, but not limited to, ICH E...Remote workPrincipalRegulatoryFlexible hours- ...Updated: Today Location: Remote, India Job ID:17977... ..., you will take a leading role in development of... ...business strategy. The Principal Medical Writer will ensure... ...data presentations, regulatory documentation, and statistical... ..., other writers, editors, physicians, and...Remote workPrincipalRegulatoryContract workWork at officeHome office
$126.9k - $215.4k
Your Role As the Senior Principal Medical Writer, you will lead the end-to-end development of complex regulatory submission documents—ensuring high communication quality, scientific... ...management. Vendor management and remote leadership. Strong communication, negotiation...Remote workPrincipalRegulatory- ...Job Description: Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases... ...· Flexible, inclusive culture — 70% remote workforce, 66% women-led teams ·...Remote workPrincipalRegulatoryContract workWork at officeWorldwideFlexible hours
- BioMarin Pharmaceutical Inc. is seeking a Principal Clinical Medical Writer to progressively develop the Medical Writing function within Development... ..., aligns with program needs, and ensures high-quality regulatory documentation across development programs. You will draft/...Remote jobPrincipalRegulatory
- Principal Medical Writer ViiV Healthcare, a global specialty HIV company,... ...Principal Medical Writer who will lead and deliver high-quality... ...for complex clinical and regulatory projects. You will work closely... ...working in multicultural or remote team settings. Proven...Remote workPrincipalRegulatoryLocal area
$128k - $160k
...Job Description Principal Medical Writer, Regulatory & Scientific Writing \n Location: Remote or Hybrid in San Diego \n Employment Type: Full time \n Reports... ...including complex submissions. You will serve as a lead on assigned projects, advise clients and...Remote workPrincipalRegulatoryFull time- ## Principal Medical Writer - Clinical FocusApply: Fully Remote: Massachusetts: Canada: United States: Full time: Posted Today... ...high quality documentation for regulatory submissions in order to help... ...Collective experience writing and leading a range of documents in their...Remote workPrincipalRegulatoryFull timeLocal areaWorldwideFlexible hours
$80.6k - $175.7k
Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UKSyneos Health is a leading fully-integrated life sciences services organization built to accelerate customer... ...* Process experience is a huge plus* Remote - Open to US, UK and CanadaAt Syneos...Remote workPrincipalRegulatoryFlexible hours- Sr Principal Medical Writer job at ICON Strategic Solutions. Remote. Sr. Principal Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... ...development of high-quality clinical and regulatory documents, ensuring clarity,...Remote jobPrincipalRegulatoryFlexible hours
- ## Principal Medical WriterApplyremote type: Fully Remotelocations: Massachusetts: France: Republic... ...plans and prepares a range of regulatory documents and medical communications to... ...years· Flexible, inclusive culture — 70% remote workforce, 66% women-led teams· Learn more...Remote workPrincipalRegulatoryContract workWork at officeWorldwideFlexible hours
- As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical... ...intelligence. What you will be doing Leading the preparation, review, and editing... ...), investigator brochures (IBs), and regulatory submissions, ensuring accuracy,...Remote jobPrincipalRegulatoryContract workFlexible hours
$132k - $151k
Principal Medical Writer - CMC Focus page is loaded## Principal Medical Writer... ...:****Job Overview:**Regulatory Writers prepare high-quality... ...Flexible, inclusive culture - 70% remote workforce, 66% women-led... ...IMPDs* Experience authoring and leading Modules 3 (e.g., Modules 3.2...Remote workPrincipalRegulatoryLocal areaWorldwideFlexible hours$75k - $90k
...We are looking for a Medical Editor to join our team. You will be responsible... ...and medical, legal, and regulatory compliance during this cycle... ...Editor. This role is open to remote candidates in the United States... ...Responsibilities Edit copy and ensure regulatory compliance...Remote workRegulatoryFull timeFreelance
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