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Medical Writing Associate Jobs in Washington (NOW HIRING)

Singh

Med Tech

Ashburn, VA

The Med Tech positionis a multifaceted role that involves being a care provider, medical aide, and ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...

Singh Development Company

Med Tech

Ashburn, VA · On-site

Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...

Singh Development Company

Med Tech

Ashburn, VA · On-site

Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...

Howard University

Medical Assistant

Washington, DC · On-site

$19 - $24/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ability to read, understand, and respond to oral and written instructions. * Associate's degree in Medical Technology, Nursing, or related field, or two (2) years related experience in a physician ...

The Sky Bridge at Town Center

Med Tech

Upper Marlboro, MD · On-site

  • Retirement

  • PTO

As a Watermark associate, you will have the opportunity to deploy your talents to their fullest as ... valid written search agreement in place for this position will be deemed the sole property of ...

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Medical Writing Associate information

See Washington salary details

$27.2K

$66.2K

$152.9K

How much do medical writing associate jobs pay per year?

As of Aug 16, 2026, the average yearly pay for medical writing associate in Washington is $66,188.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,300.00 and $78,700.00 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 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.

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 are the most commonly searched types of Medical Writing jobs in Washington?

The most popular types of Medical Writing jobs in Washington are:

Medical Writing Associate jobs near you
Infographic showing various Medical Writing Associate job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $66,188 per year, or $31.8 per hour.

Clinical Regulatory Writer, Associate Director / Manager

AstraZeneca

Gaithersburg, MD • On-site

$133K - $199K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

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

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Job Title: Clinical Regulatory Writer, Associate Director / Manager

Location: Gaithesrburg, MD- Hybrid (3 days onsite)

Introduction to role:
Are you ready to be part of the solution, turning drug development strategies into reality? As an Associate Director in Clinical Regulatory Writing, you'll 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, Associate Director, 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.

  • 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.)

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. 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

30-Jul-2026

Closing Date

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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