Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Senior/Principal Medical Editor - FSP (Regulatory Documents)

$62k - $175.7k

Syneos Health Inc

Senior/Principal Medical Editor – FSP (Regulatory Documents)

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.

We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

• Maintains strong familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance.

• Represents the editorial group in medical writing, on study teams, and in cross-departmental project teams as needed.

• Monitors timelines and budgets for assigned projects and updates the lead medical writer, project manager, and/or direct supervisor (as appropriate) if deliverables are at risk.

• Provides technical support and expertise as appropriate. Conducts training of medical editing staff and functions as a mentor. Advises medical writers, medical editors, and study teams on quality review, compilation, and editorial standards. Provides training to members of the global medical writing team in aspects relative to their roles.

• Serves as project lead for deliverables of assigned complex and/or large medical writing projects, including, but not limited to, scheduling and leading internal project-specific team meetings, organizing project-specific requirements, and ensuring all information is distributed to the editorial team and implemented within the deliverable.

• Serves as a member of the medical writing team for projects with medical writing deliverables. Provides feedback to the lead medical writer on progress of editorial process.

• Copyedits assigned documents, applying correct grammar, punctuation, spelling, and style following AMA Manual of Style or various custom style guidelines as well as established medical writing internal checklists and best practices.

• Performs quality review of assigned documents to ensure accuracy.

• Contributes to the development of process improvement tools and the development or revision of internal policies and procedures affecting editorial work.

• Manages assigned projects according to medical writing standard operating procedures and client standards, on time and on budget.

• May compile medical writing deliverables.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

$62,000.00 - $175,700.00

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

Vacancy posted 10 hours ago
Similar jobs that could be interesting for youBased on the Senior/Principal Medical Editor - FSP (Regulatory Documents) in United States vacancy
  • $62k - $175.7k

     ...Principal/Senior Medical Editor (Publications Documents) Updated: August 14, 2026 Location: Remote, NC, United States Job ID:25111527 Description Principal...  ...ensure that documents meet or exceed sponsor and regulatory requirements and guidance. Represents the editorial... 
    Document
    Principal
    Senior
    Regulatory
    Contract work
    Remote work
    Flexible hours

    Syneos Health Inc

    Morrisville, NC
    3 days ago
  • $105k - $125k

     ...Senior Regulatory Medical Writer (FSP; Remote; US)At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a...  ...a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author... 
    Document
    Senior
    Regulatory
    Temporary work
    Local area
    Remote work
    Flexible hours

    Thermo Fisher

    Framingham, MA
    4 days ago
  •  ...Parexel FSP has an exciting opportunity for a Medical Writer ! Key Accountabilities : Author Clinical Documents Gather, review, analyze, and evaluate pertinent resources to...  ...clinical documents for submission to regulatory authorities, including but not limited... 
    Document
    Senior
    Regulatory
    Interim role
    Remote work
    Flexible hours
    Remote
    29 days ago
  •  ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer/Principal Medical Writer will...  ...-quality and on-time clinical study documents. Specific responsibilities include...  ...Style Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP) and... 
    Document
    Principal
    Senior
    Regulatory
    Remote work

    Precision for Medicine

    United States
    5 days ago
  • $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 rigor, regulatory compliance, and timely delivery across international markets. Acting... 
    Document
    Principal
    Senior
    Regulatory
    Remote work

    EMD Serono, Inc.

    Billerica, MA
    5 days ago
  • Principal / Senior Medical Writer - with proven strong clinical document writing experience Syneos Health® is a leading fully-integrated life sciences services organization...  ...meetings. Adheres to established regulatory standards, including, but not limited to, ICH... 
    Document
    Principal
    Senior
    Regulatory
    Contract work
    Remote
    21 days ago
  • $80.6k - $175.7k

    Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK Syneos Health® is a leading fully-integrated life sciences services...  ...comments from the client. • Completes a variety of documents that may include clinical study protocols and clinical... 
    Document
    Principal
    Senior
    Regulatory
    Full time
    Contract work
    Remote work
    Flexible hours

    Syneos Health

    Remote
    2 days ago
  • Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the...  ...-quality and on-time clinical study documents. Specific responsibilities include clinical...  ...Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP ) and... 
    Document
    Principal
    Senior
    Regulatory
    Full time

    Precision Medicine Group

    Remote
    22 days ago
  • $115.9k - $243.9k

    Job Level: FSP Principal Biostatistician, Late Phase Location: Home-based...  ...orders.Experience with regulatory submissions.Engaging, fast-paced...  ...and other regulatory documents, e.g. NDA, DSURs, Briefing Documents...  ...of innovative medical treatments to help improve patient... 
    Document
    Principal
    Regulatory
    Full time
    Part time
    Immediate start
    Remote work
    Work from home
    Worldwide
    Flexible hours

    IQVIA

    Durham, NC
    2 days ago
  • Job Title: Senior Scientist / Principal Scientist - Biotransformation/Metabolite Identification.Location: Exton, PennsylvaniaFull-time Job...  ...Prepare and review scientific reports, presentations, and regulatory documents to ensure accuracy and compliance with industry... 
    Document
    Principal
    Senior
    Regulatory

    Frontage Laboratories

    Exton, PA
    3 days ago
  •  ...Senior/Principal Medical Writer For the past 25 years, ProPharma has improved...  ...deep domain expertise in regulatory sciences, clinical research...  ...Due to growth within the FSP Medical Writing function at...  ...Manages clinical program documents for assigned clients, such... 
    Document
    Principal
    Regulatory
    Contract work
    Work at office
    Remote work

    Avery Healthcare Group Ltd.

    United States
    3 days ago
  •  ...Reference26-00447 Job Description: The Senior Manager in Statistics responsible for perform...  ...activities in drug in-licensing, regulatory filings and marketing. Responsibilities...  ...Review study report, manuscripts and other documents related to statistics. Work on responses... 
    Document
    Principal
    Senior
    Regulatory

    Katalyst Healthcares & Life Sciences

    Paramus, NJ
    5 days ago
  • $145.82k - $182.02k

     ...Clinical Scientist to join our team. The Senior / Principal Clinical Scientist, Clinical...  ...teams, including clinical operations, regulatory affairs, and research and development,...  ...consent forms, and other study-related documents. Collaborate with principal investigators... 
    Document
    Principal
    Senior
    Regulatory

    Immunome

    Bothell, WA
    1 day ago
  •  ...Office Job Description Join Us as a Principal Clinical Trial Coordinator FSP- Make an Impact at the Forefront...  ...development of country or site‑specific documents. Support study close‑out...  ...tracking of SOPs, client directives, and regulatory guidelines at the project level.... 
    Document
    Principal
    Regulatory
    Contract work
    Work at office
    Local area

    NCBiotech

    Raleigh, NC
    2 days ago
  • Capital One is seeking a Principal Auditor to lead audits across finance, accounting, regulatory reporting, and treasury risk. You will develop engagement plans, design procedures, and document findings while coaching junior staff. The role emphasizes collaboration with... 
    Document
    Principal
    Senior
    Regulatory

    Capital One

    Mc Lean, VA
    3 days ago
  • Northrop Grumman is seeking a Senior Principal Price/Cost Proposal Analyst to support the Strike Division at...  ...extensive cost analysis, negotiation, and regulatory experience. You will evaluate proposals, build PCAR documents, and work with suppliers to ensure accurate cost... 
    Document
    Principal
    Senior
    Regulatory

    Northrop Grumman

    Palmdale, CA
    2 days ago
  •  ...solutions.Represent the architectural vision to senior collaborators and technical teams...  ...breaks between interviews, having documents read aloud or office accessibility. Please...  ...we can offer is limited by local legal, regulatory, tax, or other considerations, and where... 
    Document
    Principal
    Senior
    Regulatory
    Work at office
    Local area
    Remote work

    ARM

    San Jose, CA
    3 days ago
  •  ...Arm has an exciting opportunity for a Senior Principal Product Engineer in our Product Engineering...  ...breaks between interviews, having documents read aloud, or office accessibility....  ...can offer is limited by local legal, regulatory, tax, or other considerations, and where... 
    Document
    Principal
    Senior
    Regulatory
    Work at office
    Local area
    Relocation

    ARM

    Austin, TX
    5 days ago
  • $308.6k - $417.5k

     ...examples of support include breaks between interviews, having documents read aloud or office accessibility. Please email us about anything...  ..., the flexibility we can offer is limited by local legal, regulatory, tax, or other considerations, and where this is the case, we... 
    Document
    Principal
    Senior
    Regulatory
    Work at office
    Local area

    ARM

    Austin, TX
    3 days ago
  • $93k - $172k

     ...approve qualification and validation documents. You will perform quality oversight...  ...degree (Masters Preferred) with 8 years (Principal) or 12 years (Senior Principal) industry experience You...  ...8Date posted : 2026-06-17Profession: Regulatory & QualityEmployment type: Full time
    Document
    Principal
    Senior
    Regulatory
    Full time
    Local area

    Genentech

    Hillsboro, OR
    5 days ago
  • $132.4k - $205.1k

     ...can take you places you never expected.Senior Principal System Engineer - New Product...  ...Design ReviewsDesign systems to meet regulatory requirements.Develop and Maintain MS Project...  ...Specifications (PRS) based on Product Requirements Document (PRD)Coordinate and implement design... 
    Document
    Principal
    Senior
    Regulatory
    Local area
    Worldwide

    Tennant Company

    Golden Valley, MN
    5 days ago
  • $172.3k - $376.51k

     ...and growth-oriented, and the Senior Counsel – Corporate and Securities...  ..., policies and other documents.Representing/advocating for an...  ...business activities, transactions, regulatory matters, and organizational...  ...package that includes medical, dental, vision, life insurance... 
    Document
    Principal
    Senior
    Regulatory
    Full time
    Contract work
    Work experience placement
    Local area

    Atlantic Union Bank

    Reston, VA
    4 days ago
  •  ...Senior / Principal Scientist, QC and Analytical Development About LifeSprout...  ...spinout. We are a medical device company creating revolutionary...  ...protocols and validation documents, drafts procedures and QC...  ...functionally with R&D, manufacturing, regulatory, quality, and supply chain... 
    Document
    Principal
    Senior
    Regulatory

    LifeSprout

    Baltimore, MD
    1 day ago
  •  ...combination strategies through translational data. Contribute to regulatory documents, including INDs, clinical protocols, investigator brochures,...  ...and scientific updatesWork Hard, Stay WellComprehensive medical, dental, and vision plans for employees and their... 
    Document
    Principal
    Senior
    Regulatory
    Summer holiday
    Local area

    Neomorph

    San Diego, CA
    5 days ago
  •  ...Senior Principal Statistician, BiostatisticsJazz Pharmaceuticals is a global biopharma...  ...analysis and validation, and study documentation. The Senior Principal Statistician...  ...clinical drug supply, project management, regulatory affairs, medical writing, clinical data management,... 
    Document
    Principal
    Senior
    Regulatory
    Flexible hours

    Jazz Pharmaceutical

    Philadelphia, PA
    4 days ago
  • Syneos Health is seeking a Senior/Principal Medical Editor for Regulatory Documents, supporting FDA and EU guidelines across study teams. The role leads editorial efforts, mentors staff, and ensures high-quality regulatory writing and document standards. You will monitor... 
    Document
    Regulatory

    Syneos Health

    New York, NY
    4 days ago
  • $158.84k - $190.63k

     ...Senior Principal EngineerThis is a rare chance to serve as a top-level technical...  ...the highest levels of the regulatory process.Key responsibilities...  ...guidelines, and technical documents; build member consensus and...  ...package that includes medical, dental, vision, 401k, paid... 
    Document
    Principal
    Senior
    Regulatory
    Work at office

    EEI Corporation

    Washington DC
    4 days ago
  •  ...cleaning timelines and ensure adherence to risk mitigation plans Document and communicate findings clearly and effectively to study...  ...inspections Understanding of clinical data flow, study endpoints, and regulatory requirements Strong analytical and critical‑thinking... 
    Document
    Principal
    Senior
    Regulatory

    Jobtailor

    Raleigh, NC
    2 days ago
  • $154.4k - $242.55k

     ...DescriptionJoin Takeda as a Senior/Principal Scientist, Cell Based-...  ...stability testing, comparability, regulatory submissions, and analytical...  ..., data interpretation, documentation, and cross-functional technical...  ...eligible to participate in medical, dental, vision insurance,... 
    Document
    Principal
    Senior
    Regulatory
    Minimum wage
    Contract work
    Temporary work
    Local area

    Takeda

    Lexington, MA
    3 days ago
  •  ...Parexel FSP is looking for a CRA/Sr CRA in the...  ...with Client Procedural Documents, international guidelines...  ...study start-up and regulatory maintenance. Tasks may...  ...timely feedback to the Principal Investigator, including...  ...with local Medical Science Liaisons (MSLs... 
    Document
    Senior
    Regulatory
    Local area
    Remote work
    Flexible hours
    Shift work

    PAREXEL

    East Montpelier, VT
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Senior/Principal Medical Editor - FSP (Regulatory Documents). Be the first to apply!