2

Entry Level Regulatory Medical Writer Jobs (NOW HIRING)

OR

$95K - $210K/yr

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 ...

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

The Medical Writer, Global Medical Affairs, reports to the Director of Medical Writing and is a key ... regulatory and company policies Review author disclosures, acknowledgments, and contribution ...

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

The Medical Writer interfaces with external groups to ensure accurate and timely completion ... regulatory and company policies Review author disclosures, acknowledgments, and contribution ...

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

The Medical Writer, Global Medical Affairs, reports to the Director of Medical Writing and is a key ... regulatory and company policies Review author disclosures, acknowledgments, and contribution ...

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

The Medical Writer interfaces with external groups to ensure accurate and timely completion ... regulatory and company policies Review author disclosures, acknowledgments, and contribution ...

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

The Medical Writer interfaces with external groups to ensure accurate and timely completion ... regulatory and company policies Review author disclosures, acknowledgments, and contribution ...

Medical Writer

$90K - $105K/yr

The Medical Writer is responsible for creating communications materials including but not limited ... Follows governmental regulations and company SOPs for document preparation. Information Security ...

Medical Writer

$78K - $102K/yr

Advance your medical writing career with purpose and impact. Work shouldn't just be something we do ... regulations. * Create high-quality, scientifically accurate, and compliant content to meet client ...

Groton, CT Duration: 3 years+ Our client is looking to hire the Medical Writer Company is looking ... Skills of Common Technical Document Efficacy components that are compliant with regulations, ICH ...

Medical Writer

Charleston, WV · On-site

$85K - $100K/yr

The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ... Follow AMA/AP style, brand guidelines, and all relevant industry regulations, including fair ...

In addition, you may have the chance to work on regulatory documents, lay summaries and policy ... Positions are available for those looking for an entry-level role in the field as well as those ...

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ... Follow AMA/AP style, brand guidelines, and all relevant industry regulations, including fair ...

Prepares scientific and regulatory documents on behalf of government and private sector clients for ... Superior writing skills that require moderate to minimal editing. Knowledge of regulatory ...

Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...

Review medical scientific literature, analyze clinical risk and provide benefit/risk assessments, write, review, and edit CERs to comply with international regulations; write and update coherent and ...

next page

Showing results 1-20

Entry Level Regulatory Medical Writer information

See salary details

$14

$38

$57

How much do entry level regulatory medical writer jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for entry level 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 Entry Level Regulatory Medical Writer vs Regulatory Medical Writer?

AspectEntry Level Regulatory Medical WriterRegulatory Medical Writer
Required CredentialsBachelor's degree, life sciences background, some familiarity with regulationsBachelor's or higher in life sciences, with more experience in regulatory writing
Work EnvironmentEntry-level, training-focused, often in pharmaceutical or biotech companiesMore experienced, may lead projects, work in similar settings
Employer & Industry UsagePharmaceutical, biotech, CROs, regulatory agenciesPharmaceutical, biotech, CROs, regulatory agencies

The main difference is experience level and familiarity with regulatory processes. Entry Level Regulatory Medical Writers are just starting their careers and require training, while Regulatory Medical Writers have more experience and handle complex documentation independently.

What cities are hiring for Entry Level Regulatory Medical Writer jobs? Cities with the most Entry Level 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 Entry Level Regulatory Medical Writer jobs? States with the most job openings for Entry Level Regulatory Medical Writer jobs include:
Sr. Principal Regulatory Medical Writer - Oncology Preferred

Sr. Principal Regulatory Medical Writer - Oncology Preferred

Syneoshealth

OR

$95K - $210K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 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.


What Syneos Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom