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Live In Regulatory Medical Writer Jobs (NOW HIRING)

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

Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services ... Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you ...

Medical Writing Manager

Pueblo, CO · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Carmel, IN · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Newark, NJ · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Quincy, MA · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

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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 Aug 7, 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:
What states have the most Live In Regulatory Medical Writer jobs? States with the most job openings for Live In Regulatory Medical Writer jobs include:

Senior Regulatory Medical Writer, Client-embedded, FSP

Thermo Fisher Scientific

Framingham, MA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 536 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Senior Regulatory Medical Writer (FSP; Remote; US)

At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Summarized Purpose:

We are excited to expand our Medical Writing FSP Team and are seeking candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. The Senior Medical Writer may assist the program manager. The successful candidate will have a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.

Essential Functions:

  • Serves as a primary author who writes and provides input on routine clinical documents such as clinical study reports and study protocols and summarizes data from clinical studies.
  • Serve as a primary author who writes complex clinical and scientific and program level documents, such as IBs, bioassay reports, INDs, and MAAs.
  • Collaborate with cross-functional teams to gather necessary information and ensure the accuracy and completeness of documents.
  • Ensure documents align with regulatory guidelines, company standards, and industry best practices.
  • Provide input on document content, structure, and presentation.
  • Review and provide feedback on documents prepared by other team members.
  • Manage timelines and deliverables for assigned projects.
  • Mentor and provide oversight to junior medical writers and ensure high-quality deliverables
  • Stay current with industry trends, guidelines, and regulatory requirements.

Education and Experience:

  • Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
  • Experience working in the pharmaceutical/CRO industry preferred.
  • Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.
  • In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, and Abilities:

  • Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
  • Strong project management skills
  • Excellent interpersonal skills including problem solving.
  • Strong negotiation skills
  • Excellent oral and written communication skills with strong presentation skills
  • Significant knowledge of global, regional, national, and other document development guidelines
  • Great judgment and decision-making skills
  • Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g., Excel, Outlook).

What We Offer:

At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development program, ensuring you reach your potential.  

As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We have grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.

Compensation and Benefits

The salary range estimated for this position based in Massachusetts is $105,000.00–$125,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards


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