ZipRecruiter

Log In

1

Medical Writing Fellowship Jobs (NOW HIRING)

Synterex, Inc.

Senior Medical Writer

Princeton, NJ · On-site

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships. #J-18808-Ljbffr

Synterex

Senior Medical Writer

Princeton, NJ · Remote

Synterex is seeking an organized, motivated, and collaborative individual for our medical writing ... For more information, please visit www.synterex.com/fellowships -internships.

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Beyond your individual contributions, you will mentor and develop fellow writers, champion best ...

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Beyond your individual contributions, you will mentor and develop fellow writers, champion best ...

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Beyond your individual contributions, you will mentor and develop fellow writers, champion best ...

Synterex

Senior Medical Writer

Princeton, NJ · On-site

$120K/yr

Synterex is seeking an organized, motivated, and collaborative individual for our medical writing ... For more information, please visit www.synterex.com/fellowships-internships.

Synterex

SeniorMedical Writer

Princeton, NJ · On-site +1

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships.

Synterex

SeniorMedical Writer

NJ · Remote

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships.

next page

Showing results 1-20

All JobsEducation JobsBusiness Education JobsScientific Writer JobsMedical Writing Fellowship Jobs

Medical Writing Fellowship information

See salary details

$11

$46

$78

How much do medical writing fellowship jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for medical writing fellowship in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What is a medical writing fellowship?

A Medical Writing Fellowship is a structured training program designed to provide early-career professionals with hands-on experience in medical writing. Fellows typically work under the guidance of experienced writers and editors, learning to create regulatory documents, clinical study reports, manuscripts, and other scientific materials. These fellowships often last 1-2 years and offer mentorship, networking opportunities, and exposure to various therapeutic areas. The goal is to prepare participants for a successful career in medical writing within the pharmaceutical, biotechnology, or healthcare communication industries.

What types of projects can a medical writing fellow expect to work on during the fellowship, and how does this experience support future career growth?

As a Medical Writing Fellow, you can expect to engage in a variety of projects such as drafting clinical study reports, preparing regulatory submission documents, developing manuscripts for publication, and creating educational materials for healthcare professionals. These experiences provide hands-on exposure to different medical writing formats and therapeutic areas, helping you build a diverse portfolio. Collaborating closely with cross-functional teams like clinical researchers, regulatory affairs, and subject matter experts also hones your communication and project management skills. This multifaceted exposure is highly valued by employers and sets a strong foundation for advancement into senior medical writing or leadership roles.

What are the key skills and qualifications needed to thrive as a medical writing fellow, and why are they important?

To thrive as a Medical Writing Fellow, you need a strong background in life sciences or medicine, excellent writing skills, and a keen attention to detail, often supported by an advanced degree such as a PhD, PharmD, or MD. Familiarity with referencing software (like EndNote), document management systems, and knowledge of regulatory guidelines (such as ICH or GPP) are typically required. Outstanding communication, time management, and adaptability are crucial soft skills in this position. These skills ensure the accurate, clear, and timely delivery of complex scientific information for regulatory, educational, or publication purposes.

What is the difference between Medical Writing Fellowship vs Medical Writer?

AspectMedical Writing FellowshipMedical Writer
CredentialsTypically requires a degree in life sciences or related field; some fellowships may require prior writing experienceRequires a degree in life sciences, healthcare, or related field; certification is optional but beneficial
Work EnvironmentOften in academic, pharmaceutical, or biotech settings; focused on training and mentorshipIn-house or freelance; involved in producing clinical, regulatory, or marketing documents
Industry UsageUsed as a training program for aspiring medical writersProfessional role for experienced or entry-level writers in healthcare and pharma

In summary, a Medical Writing Fellowship is a training program designed to develop skills in aspiring medical writers, often within academic or industry settings. A Medical Writer is a professional who produces scientific and regulatory documents, with varying levels of experience. Fellowships serve as a stepping stone into the medical writing profession, whereas medical writers are actively engaged in document creation across healthcare sectors.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. The role often requires strong writing skills, knowledge of medical terminology, and familiarity with regulatory guidelines.

How can I get into a medical writing fellowship with no experience?

Medical writing fellowships often accept candidates with strong scientific backgrounds, such as degrees in life sciences or related fields, even without prior experience. Gaining skills in scientific communication, familiarity with medical terminology, and proficiency in tools like Microsoft Word or reference management software can improve your chances; completing relevant courses or certifications can also be beneficial.

Is there a demand for medical writing fellows?

There is a growing demand for medical writing fellows as the healthcare and pharmaceutical industries require skilled professionals to create clinical, regulatory, and scientific documentation. These roles often require strong writing skills, knowledge of medical terminology, and familiarity with industry regulations, making them valuable in the healthcare communication field.
More about Medical Writing Fellowship jobs

What cities are hiring for Medical Writing Fellowship jobs?

Cities with the most Medical Writing Fellowship job openings:

What states have the most Medical Writing Fellowship jobs?

States with the most job openings for Medical Writing Fellowship jobs include:

What are popular job titles related to Medical Writing Fellowship jobs?

For Medical Writing Fellowship jobs, the most frequently searched job titles are:

Medical Writing Fellowship jobs near you
Infographic showing various Medical Writing Fellowship job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Senior Principal Medical Writer

North Billerica, MA • On-site, Remote

EMD Group
See more jobs at EMD Groupexternal

$126K - $215K/yr

Full-time

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Senior Principal Medical Writer

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 as the primary medical writing lead within cross-functional teams, you will define document strategy, shape submission timelines, and align stakeholders across clinical, regulatory affairs, pharmacovigilance, and statistics. Beyond your individual contributions, you will mentor and develop fellow writers, champion best practices, and drive consistency and quality across deliverables. This is a role for a seasoned professional who combines deep medical writing expertise with the ability to influence decisions, lead without authority, and deliver with precision on programs that directly advance patient health.

Location: Hybrid – 3x/week onsite in Billerica, MA required.

Key Responsibilities:

  • Lead medical writing efforts for global, priority programs across the full regulatory documentation suite (protocols, clinical study reports, Investigator's Brochures, briefing books, clinical summaries, pediatric plans, authority responses, etc.).
  • Act as Lead Writer/oversight for clinical sections of regulatory dossiers (eCTD) for global market approvals.
  • Represent Medical Writing in cross-functional teams; participate in governance and project meetings.
  • Define and implement document strategy, resource needs, and timelines; manage deliverables from vendors and external writers as needed.
  • Mentor and develop writers; drive adoption of MW best practices and standards.
  • Manage documentation strategy, quality, and consistency across indications; ensure alignment with regulatory expectations.
  • Coordinate with cross-functional teams (clinical, pharmacovigilance, regulatory affairs, statistics) to ensure timely and compliant delivery.

Who You Are:

Minimum Qualifications:

  • Bachelor's degree in a scientific or writing discipline; Master's or PhD preferred.
  • 5–8 years of relevant medical writing experience in pharma/biotech, with strong regulatory documentation background.
  • Proven ability to lead multiple writers and coordinate vendor resources for regulatory submissions (IND/IMPD, bridging documents, briefing books, etc.).
  • Solid CTD/CTD-like knowledge; experience across multiple markets is a plus.
  • Excellent written and verbal English; strong presentation and collaboration skills.
  • Ability to travel as needed.

Preferred Qualifications:

  • Experience with country-specific submissions and post-approval documents
  • Proficiency with document management systems, SharePoint, and standard MW templates
  • Familiarity with industry best practices and evolving regulatory guidelines
  • Strategic document planning and cross-functional leadership
  • Deep knowledge of regulatory submission requirements and lifecycle management
  • Vendor management and remote leadership
  • Strong communication, negotiation, and stakeholder management
  • High attention to quality, accuracy, and compliance

Pay Range for this position: $126,900 – 215,400

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.

This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Apply