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Live In Regulatory Medical Writer Jobs (NOW HIRING)

OR · On-site

$95K - $210K/yr

Sr. Principal Regulatory Medical Writer - Oncology Preferred Syneos Health is a leading fully ... Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you ...

Significant experience in medical writing, particularly in regulatory submissions and clinical documentation * Strong understanding of regulatory requirements and industry standards for clinical ...

... regulatory and company policies Review author disclosures, acknowledgments, and contribution ... Background in medical affairs, clinical research, or evidence generation is highly preferred

All members of our medical team are live in Boston, MA. Responsibilities and Duties Critically ... regulatory review for assigned projects, incorporating feedback and preparing projects for ...

Medical Writer

$90K - $105K/yr

The Medical Writer is engaged in all aspects of client interactions from initial kickoff through ... Follows governmental regulations and company SOPs for document preparation. Information Security ...

Operates in compliance with applicable Medical Information governance, SOPs, and regulatory ... Strong written communication skills, with demonstrated experience in scientific or medical writing ...

... and regulatory submissions (e.g. FDA, PMA, CE marking technical documentation). * Involved in ... medical writing experience in the medical device or pharmaceutical industry or 7+ years general ...

... rooted in strong science and decades of regulatory experience - that will assist our clients in ... Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the ...

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... In addition, you may have the chance to work on regulatory documents, lay summaries and policy ...

Prepares scientific and regulatory documents on behalf of government and private sector clients for ... This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working ...

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Strong expertise in clinical development, regulatory writing standards, and cross-functional ... Medical Writing ───── Requirements ───── Bachelor's degree or higher in a ...

The Medical Writer collaborates with members of cross-functional teams to prepare high-quality ... in one or more of the oncology or rare diseases therapeutic areas; * 3 -8 years of regulatory ...

... regulations; write and update coherent and convincing CERs and PMCF Reports by organizing and ... PhD degree in Biomedical Engineering or related field and 1 year of experience writing and ...

Analyst/Medical Writer

Boston, MA · Hybrid

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... In addition, you may have the chance to work on regulatory documents, lay summaries and policy ...

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Live In Regulatory Medical Writer information

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How much do live in regulatory medical writer jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for live in regulatory medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Live In Regulatory Medical Writer vs Regulatory Medical Writer?

AspectLive In Regulatory Medical WriterRegulatory Medical Writer
CredentialsTypically requires a life sciences degree and medical writing certificationSame as Live In role, often with additional regulatory training
Work EnvironmentUsually based at a single location, living on-site or nearbyOffice-based or remote, depending on employer
Employer & IndustryPharmaceutical, biotech companies, or CROsPharmaceutical, biotech, or regulatory agencies
Search & Comparison IntentOften searched by those seeking on-site or live-in rolesMore general, including remote or office roles

Live In Regulatory Medical Writers focus on on-site, live-in roles within pharmaceutical or biotech companies, requiring specific certifications and a preference for on-location work. Regulatory Medical Writers may work remotely or in-office, with similar qualifications, but without the live-in component. The main difference lies in the work setting and living arrangements.

What cities are hiring for Live In Regulatory Medical Writer jobs? Cities with the most Live In Regulatory Medical Writer job openings:
What are the most commonly searched types of Regulatory Medical Writer jobs? The most popular types of Regulatory Medical Writer jobs are:
Sr. Principal Regulatory Medical Writer - Oncology Preferred

Sr. Principal Regulatory Medical Writer - Oncology Preferred

Syneoshealth

OR • On-site

$95K - $210K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago


Syneos Health rating

8.5

Company rating: 8.5 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

18th of 71 rated pharmaceutical


Job description

Sr. Principal Regulatory Medical Writer - Oncology Preferred

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

  • Develop regulatory documents for submission to regulatory agencies globallyincluding Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives.
  • Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations.
  • Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents.
  • Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate.
  • eCTD submission experience preferred.

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:

$95,000.00 - $210,900.00

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.

Get to know Syneos Health


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.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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