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 ...
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 ...
Significant experience in medical writing, particularly in regulatory submissions and clinical documentation * Strong understanding of regulatory requirements and industry standards for clinical ...
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin ... PRINCIPAL MEDICAL WRITER - REGULATORY AND MEDICAL WRITING SUMMARY: The Principal Medical Writer ...
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin ... PRINCIPAL MEDICAL WRITER - REGULATORY AND MEDICAL WRITING SUMMARY: The Principal Medical Writer ...
Senior Medical Writer (Remote)
OR · On-site +1
This role will specialize in writing, editing, and reviewing clinical regulatory documents as well as support and execute general medical writing activities. These activities include performing ...
Senior Medical Writer (Remote)
OR · On-site +1
This role will specialize in writing, editing, and reviewing clinical regulatory documents as well as support and execute general medical writing activities. These activities include performing ...
Medical Writer
Maple Grove, MN · On-site
MDR (Medical Device Regulations) * EU (European Union) * Literature Review (e.g., PubMed ... Degree in Life Sciences (Advanced degree preferred). * Experience in Medical Device or ...
Medical Writer
Maple Grove, MN · On-site
MDR (Medical Device Regulations) * EU (European Union) * Literature Review (e.g., PubMed ... Degree in Life Sciences (Advanced degree preferred). * Experience in Medical Device or ...
Senior Medical Writer - Medical Communications
Philadelphia, PA · Hybrid
$110K/yr
... in science and regulatory, medical strategy, medical communications, and value, access and ... Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned ...
Senior Medical Writer - Medical Communications
Philadelphia, PA · Hybrid
$110K/yr
... in science and regulatory, medical strategy, medical communications, and value, access and ... Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned ...
Additionally, must posess the ability to guide and assists medical writers in the writing of documents that are components of clinical/ regulatory approval applications for new biologics or NME ...
Additionally, must posess the ability to guide and assists medical writers in the writing of documents that are components of clinical/ regulatory approval applications for new biologics or NME ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Independently authors (writes/edits) high-quality medical writing deliverables (i.e., clinical ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Independently authors (writes/edits) high-quality medical writing deliverables (i.e., clinical ...
Medical Writer
Bethesda, MD · On-site
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 ...
Medical Writer
Bethesda, MD · On-site
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 ...
OR · On-site
... 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 ...
OR · On-site
... 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 ...
We provide quality resources in four specialty areas: Information Technology (IT), Clinical ... Knowledge of regulatory requirements preferred. Additional Information We do have referral bonus of ...
We provide quality resources in four specialty areas: Information Technology (IT), Clinical ... Knowledge of regulatory requirements preferred. Additional Information We do have referral bonus of ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Strives to complete medical writing deliverables on time and within budget. * With minimal ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Strives to complete medical writing deliverables on time and within budget. * With minimal ...
Senior Medical Writer (Remote)
Canton, MI · On-site
... 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 ...
Quick apply
Senior Medical Writer (Remote)
Canton, MI · On-site
... 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 ...
Principal Medical Writer
$95K - $105K/yr
In addition to representing the Clinical Communications team as a content expert, the Principal ... legal/regulatory (MLR) review process requirements. * Medical Event Attendance: * Attend live ...
Principal Medical Writer
$95K - $105K/yr
In addition to representing the Clinical Communications team as a content expert, the Principal ... legal/regulatory (MLR) review process requirements. * Medical Event Attendance: * Attend live ...
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 ...
Quick apply
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 ...
Senior Medical Writer
OR · On-site +1
... Medical Writing ... The individual will complete accurate, high quality, and regulatory compliant documents in support ...
Senior Medical Writer
OR · On-site +1
... Medical Writing ... The individual will complete accurate, high quality, and regulatory compliant documents in support ...
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 ...
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 ...
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 ...
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 ...
Senior Medical Writer
Durham, NC · On-site
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or ...
Senior Medical Writer
Durham, NC · On-site
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or ...
Medical Writer II
Plymouth, MN · Hybrid
$115K - $125K/yr
... in the development and execution of clinical, scientific, and regulatory documents and ... We do that today by helping people with pelvic and gastrointestinal conditions live normal lives ...
Medical Writer II
Plymouth, MN · Hybrid
$115K - $125K/yr
... in the development and execution of clinical, scientific, and regulatory documents and ... We do that today by helping people with pelvic and gastrointestinal conditions live normal lives ...
Live In Regulatory Medical Writer information
See salary details
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
How much do live in regulatory medical writer jobs pay per hour?
What is the difference between Live In Regulatory Medical Writer vs Regulatory Medical Writer?
| Aspect | Live In Regulatory Medical Writer | Regulatory Medical Writer |
|---|---|---|
| Credentials | Typically requires a life sciences degree and medical writing certification | Same as Live In role, often with additional regulatory training |
| Work Environment | Usually based at a single location, living on-site or nearby | Office-based or remote, depending on employer |
| Employer & Industry | Pharmaceutical, biotech companies, or CROs | Pharmaceutical, biotech, or regulatory agencies |
| Search & Comparison Intent | Often searched by those seeking on-site or live-in roles | More 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.
$95K - $210K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 3 days ago
Syneos Health rating
8.5
Based on 19 frontline employees who took The Breakroom Quiz
18th of 71 rated pharmaceutical
Job description
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 - $210,900.00The 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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About Syneos Health
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Morrisville, NC, US