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Senior Medical Writer Jobs in Silver Spring, MD (NOW HIRING)

CEDENT

Senior Medical Writer

Rockville, MD · On-site

The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related ...

MMS

Senior Medical Writer (Remote)

Dundalk, MD · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

RELI Group Inc.

Senior Medical Coder

Baltimore, MD · On-site +1

$65K - $75K/yr

We are seeking an experienced and detail-oriented Senior Medical Coder to support our Medicare Part ... Perform Medical Record Dispute and Appeal reviews including technical writing per Part C guidelines.

RELI Group, Inc.

Senior Medical Coder

Windsor Mill, MD · On-site

$19 - $25.50/hr

We are seeking an experienced and detail-oriented Senior Medical Coder to support our Medicare Part ... Perform Medical Record Dispute and Appeal reviews including technical writing per Part C guidelines.

RELI Group

Senior Medical Coder

Baltimore, MD · On-site +1

$65K - $75K/yr

We are seeking an experienced and detail-oriented Senior Medical Coder to support our Medicare Part ... Perform Medical Record Dispute and Appeal reviews including technical writing per Part C guidelines.

RELI GROUP INC

Senior Medical Coder

Baltimore, MD

$65K/yr

We are seeking an experienced and detail-oriented Senior Medical Coder to support our Medicare Part ... Perform Medical Record Dispute and Appeal reviews including technical writing per Part C guidelines.

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Senior Medical Writer information

See Silver Spring, MD salary details

$36.2K

$141.9K

$255.9K

How much do senior medical writer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for senior medical writer in Silver Spring, MD is $141,924.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,500.00 and $171,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior medical writer?

To thrive as a Senior Medical Writer, you need advanced writing and editing skills, a thorough understanding of scientific and medical concepts, and typically a degree in a life science or related field. Familiarity with referencing tools (like EndNote), document management systems, and compliance with regulatory guidelines (such as ICH or FDA standards) is often required. Strong attention to detail, project management abilities, and the capacity to communicate complex ideas clearly are important soft skills for this position. These competencies ensure accurate, high-quality medical content that meets industry standards and supports effective communication among healthcare professionals and stakeholders.

What is a senior medical writer?

A Senior Medical Writer is responsible for creating clear, accurate, and compliant medical documents, including regulatory submissions, clinical study reports, and scientific publications. They work closely with cross-functional teams, such as medical affairs, regulatory affairs, and clinical teams, to ensure high-quality content. Senior Medical Writers also review and edit documents for consistency, clarity, and adherence to industry guidelines. Often, they mentor junior writers and contribute to process improvements within the medical writing team.

What are some common challenges faced by senior medical writers, and how can they be addressed?

Senior Medical Writers often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring adherence to strict regulatory requirements. To navigate these challenges, it's essential to have strong organizational skills, effective communication with project teams, and a solid grasp of industry guidelines. Many Senior Medical Writers find that staying current with new regulations, participating in ongoing professional development, and leveraging collaborative tools help streamline the workflow. By proactively addressing these challenges, writers can maintain accuracy and efficiency while contributing valuable expertise to cross-functional teams.

What are the most commonly searched types of Medical Writer jobs in Silver Spring, MD? The most popular types of Medical Writer jobs in Silver Spring, MD are:
What are popular job titles related to Senior Medical Writer jobs in Silver Spring, MD? For Senior Medical Writer jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Senior Medical Writer jobs in Silver Spring, MD look for? The top searched job categories for Senior Medical Writer jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Senior Medical Writer jobs? Cities near Silver Spring, MD with the most Senior Medical Writer job openings:
Senior Medical Writer jobs near you
Infographic showing various Senior Medical Writer job openings in Silver Spring, MD as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $141,924 per year, or $68.2 per hour.

Senior Medical Writer

CEDENT

Rockville, MD • On-site

Full-time

Re-posted 20 days ago

Job description

The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related clinical documents within agreed-upon timelines.
Essential Duties and Responsibilities:
  • Prepares, edits, and finalizes protocols, investigator brochures, synopses, regulatory documents and related clinical documents, such as abstracts, posters, presentations, and manuscripts
  • Participates in scientific communication planning, including development of strategic medical communication plans
  • Partners with the study biostatistician to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings (TFLs), and narrative planning for relevant documents
  • Works closely with the study team to ensure that results and messages in clinical documents accurately reflect the data in TFLs and other information sources
  • Schedules and conducts document-related meetings including the preparation of pre-meeting agenda, key data points for discussion, and post-meeting minutes
  • Collaborate with clinicians, clinical scientists, biostatisticians, and pharmacokinetics to interpret study results and ensure study results and statistical interpretations are accurately and clearly reflected in relevant documents
  • Manages the document review process ensuring conflicting comments are appropriately addressed
  • Completes documents according to agreed-upon timelines and follow-up with the study team as needed to meet internal and external timeline commitments, and to ensure SOP and regulatory compliance and reach consensus on timelines for deliverables
  • Understands the functions and roles within the study team and aligns with them in delivery of documents to meet project-related goals and to meet external results disclosure obligations
  • Manages all aspects of outsourced or internal CSR production and ensures project delivery
  • Ensures that medical writing deliverables conform to the International Conference on Harmonization (ICH) and other relevant regulatory guidelines
  • Creates and maintains standard operating procedures and work instructions for preparation and maintenance of compliant medical writing deliverables
  • Ensures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in agreed document management system
  • Ensures that appropriate documented quality control (QC) checks are performed on medical writing deliverables, responds to findings, and recommends quality process improvements
  • Suggests or identifies changes, modifications, and improvements to the document preparation processes and templates to improve quality, efficiency, and productivity
  • Aligning with department management to set strategy for meeting department goals
Qualifications:
  • Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing
  • Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; attentive to details
  • Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within agreed internal and regulatory timelines; monitor and communicate progress against milestones; escalate complex issues appropriately.
  • Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members
  • Ability to utilize a balanced approach to problems, using flexibility and persistence as appropriate
  • Read, write and speak fluent English, excellent verbal and written communication skills
  • Excellent ability to interpret and present scientific and clinical trial data and understand statistical analyses.
  • Excellent writing skills coupled with knowledge of the drug development process and regulatory guidelines.
  • Effective collaborator with ability to foster strong working relationships and build consensus among colleagues on cross-functional teams.
  • Initiative and ability to handle a variety of projects simultaneously.
  • Excellent interpersonal and communication skills.
  • Advanced knowledge of clinical and regulatory documents and publication practices including GCP, ICH, ICMJE, and CONSORT.
Education/Experience:
  • (BA/BS) +8 years, (MS) +5 years, (Ph.D. or PharmD) Doctoral Degree+2 years of relevant corporate medical writing experience in the pharmaceutical industry, especially writing in one or more of the oncology or rare diseases therapeutic areas;
  • 3 -8 years of regulatory writing and submission experience
  • An understanding of the drug development process
  • Broad experience managing the medical writing responsibilities associated with multiple studies at various stages
  • Experience in interacting with cross-functional study team members
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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