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Medical Writing Associate Jobs (NOW HIRING)

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

Our associates come from all backgrounds, sharing one key quality: determination to succeed. We ... of writing/editing, * Provide training and mentorship to junior Medical Writers and Editors ...

Lilly

OR

The Associate Director, GMI is responsible for developing, influencing, and delivering a Global ... Ensure unsolicited verbal and written Medical Information inquiries from HCPs and consumers are ...

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

Our associates come from all backgrounds, sharing one key quality: determination to succeed. We ... This is more than writing - it's about shaping content that informs, educates, and drives ...

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Medical Writing Associate information

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$24K

$58.4K

$135K

How much do medical writing associate jobs pay per year?

As of May 30, 2026, the average yearly pay for medical writing associate in the United States is $58,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,500.00 and $69,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Writing Associate, and why are they important?

To thrive as a Medical Writing Associate, you need a solid background in life sciences or pharmacy, strong writing skills, and familiarity with medical terminology, often supported by a relevant degree. Proficiency in Microsoft Office, reference management software, and knowledge of regulatory submission systems are commonly required. Attention to detail, organization, and the ability to communicate complex information clearly are standout soft skills for this role. These abilities ensure accuracy, compliance, and effective communication of scientific data in regulatory and clinical documents.

What are some typical challenges faced by Medical Writing Associates when working on regulatory submission documents?

Medical Writing Associates often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring compliance with strict regulatory guidelines. Collaboration with cross-functional teams—including clinical researchers, statisticians, and regulatory affairs professionals—is essential to clarify data and maintain consistency throughout documents. Attention to detail and the ability to adapt to evolving industry standards are crucial for producing high-quality submissions that meet both regulatory requirements and client expectations.

What is a Medical Writing Associate?

A Medical Writing Associate is a professional who creates, edits, and reviews scientific documents related to medicine, healthcare, and clinical research. They are often responsible for preparing regulatory documents, clinical study reports, manuscripts, and other materials that communicate complex medical information clearly and accurately. Medical Writing Associates work closely with researchers, clinicians, and regulatory teams to ensure that documents comply with industry standards and regulatory requirements. This role is essential in the pharmaceutical, biotechnology, and healthcare industries to support drug development and ensure clear communication of scientific data.

What does an associate medical writer do?

An associate medical writer is responsible for creating clear, accurate scientific documents such as clinical study reports, regulatory submissions, and manuscripts under the supervision of senior writers. They review medical data, ensure compliance with industry guidelines, and often use tools like reference management software to support their writing tasks.

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

AspectMedical Writing AssociateMedical Writer
Required CredentialsBachelor's degree in life sciences or related field; some roles may require certificationAdvanced degree (Master's or PhD) often preferred; strong writing and scientific background
Work EnvironmentPharmaceutical or biotech companies, CROs, or medical communication agenciesPharmaceutical companies, medical communication firms, or freelance
Employer & Industry UsageEntry to mid-level role supporting medical writing tasksSenior or specialized medical writing tasks, including regulatory documents

The Medical Writing Associate typically supports medical writing projects with a focus on assisting senior writers, while Medical Writers handle more complex, regulatory, or publication writing tasks. Both roles are essential in the medical communication industry, with the associate position often serving as a stepping stone to a full Medical Writer role.

More about Medical Writing Associate jobs
What cities are hiring for Medical Writing Associate jobs? Cities with the most Medical Writing Associate job openings:
What are the most commonly searched types of Medical Writing jobs? The most popular types of Medical Writing jobs are:
What states have the most Medical Writing Associate jobs? States with the most job openings for Medical Writing Associate jobs include:
What job categories do people searching Medical Writing Associate jobs look for? The top searched job categories for Medical Writing Associate jobs are:
Medical Writing Associate jobs near you
Infographic showing various Medical Writing Associate job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 87% Full Time, and 12% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $58,439 per year, or $28.1 per hour.
Clinical Regulatory Writer (Associate Director or Manager)

Clinical Regulatory Writer (Associate Director or Manager)

AstraZeneca

Boston, MA • On-site

$169.94K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 70 rated pharmaceutical

Job description

Job Title: Clinical Regulatory Writer, Associate Director or Manager
Location: Boston, MA - Hybrid (3 days onsite)
Introduction to role:
Are you ready to be part of the solution, turning drug development strategies into reality? As a Clinical Regulatory Writer, you will play a pivotal role in translating life-changing science into medicines. Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We support AstraZeneca's core therapeutic areas across all phases of clinical development, striving for excellence in communication to achieve successful submissions and approvals.
Accountabilities:
As a Clinical Regulatory Writer, you will:
  • Independently manage clinical regulatory writing activities across a complex portfolio of work.
  • Author the most complex clinical-regulatory documents within a program, ensuring regulatory, technical, and quality standards are met.
  • Provide strategic communications leadership to projects, establishing communication standards and advocating for quality and efficiency.
  • Drive the development of the clinical Submission Communication Strategy (cSCS) when acting as a submission lead.
  • Lead internal/external authoring teams and partner with vendor medical writers to ensure timely and quality delivery.
  • Interpret complex data and information, condensing it into clear, concise messages that meet customer information requirements.
  • Demonstrate strategic thinking and review capabilities.
  • Collaborate proactively with other functions at the program level.
  • Support the development of Clinical Regulatory Writing Managers.
  • Drive continuous improvement and operational excellence from a communications leadership perspective.
    Essential Skills/Experience:
  • Education/Experience required:
    Associate Director level : BS Life Sciences degree or simiilar, 7+ yrs medical writing experience in pharmaceutical industry or CRO.
  • Manager level: BS Life Sciences degree or simiilar, 2-7+ yrs medical writing experience in pharmaceutical industry or CRO
  • Ability to advise and lead communication projects.
  • Understand drug development and communication process from development, launch through life cycle management.
  • In-depth knowledge of the technical and regulatory requirements related to the role.

Desirable Skills/Experience:
  • Advanced degree in a scientific discipline (Ph.D.)
  • Experience with CSR, CTD module 2 summaries
  • Experience leading clinical submission (NDA/BLA/MAA)
  • Experience developing clinical submission communication strategy

This is a Hybrid role - minimum requirment 3 days per week onsite
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
AstraZeneca is where innovation meets collaboration. We harness diverse knowledge to move with agility, working seamlessly across functions globally. Our team is empowered to make quick decisions, influencing drug development strategy at all levels. With a science-driven approach, we bring life-changing medicines to patients, constantly asking questions and trying new things. Your professional growth is passionately supported here, with opportunities to work on projects at all stages of development.
Ready to make an impact? Apply now and be part of our dynamic team!
The annual base pay (or hourly rate of compensation) for this position ranges from $133,042.40 - $199,563.60 USD Annual for Associate Director level, and $ 113,293.60 - $169,940.40 USD Annual for Manager level. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
13-May-2026
Closing Date
31-May-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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