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Senior Medical Writer Jobs (NOW HIRING)

Veristat

The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

Veristat

The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

Parexel

Senior Medical Writer - FSP

Parexel FSP has an exciting opportunity for a Medical Writer ! Key Accountabilities : Author Clinical Documents * Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and ...

MMS

Senior Medical Writer (Remote)

Bridgeport, CT · 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 ...

MMS

Senior Medical Writer (Remote)

Miami, FL · 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 ...

MMS

Senior Medical Writer (Remote)

Zionsville, IN · 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 ...

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$137.3K

$247.5K

How much do senior medical writer jobs pay per year?

As of Aug 12, 2026, the average yearly pay for senior medical writer in the United States is $137,286.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $166,000.00 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.

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Senior Medical Writer jobs near you
Infographic showing various Senior Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $137,286 per year, or $66 per hour.

Senior Medical Writer (Oncology)

MJH Life Sciences

Cranbury, NJ • On-site

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 15 days ago

Job description

At MJH Life Sciences our success is measured by your success! If you set your standards high and want to contribute to a winning team, we'll provide you with every opportunity to help grow our company and your career. Our associates come from all backgrounds, sharing one key quality: determination to succeed. We value being Service Focused, having a Passion for Winning, Innovation, Respect, Integrity, and Teamwork. Nothing means more to us than hiring people with these attributes. If you believe you're right for the job, this is the place to prove it!
Position Overview: As a Senior Medical Writer in the Clinical Communications team, you will be a pivotal player in crafting high-quality, scientifically accurate content aimed at educating oncology care providers. Your work will directly contribute to improving patient care outcomes in the field of oncology. You will collaborate closely with a Scientific Director (SD) and an internal team to develop content across various mediums, including print, digital, video, and live events.
Key Responsibilities:
  • Content Development:

  • Perform extensive literature reviews on various disease states, therapeutic advancements, and clinical data.

  • Develop high-quality medical and scientific content for print, digital, video, and event deliverables targeted at oncology professionals.

  • Create content that is aligned with the strategic objectives of the activity, including manuscripts, slide decks, discussion guides, and video-based educational tools.

  • Ensure the scientific and clinical accuracy of all content through a global fact-check of referenced literature and appropriate annotation following AMA style (11th edition) and in-house guidelines.

  • Review and edit content at multiple stages, ensuring consistency, accuracy, and relevance for the target audience.

  • Independently address and incorporate feedback from clients, peer reviewers, and faculty authors throughout the content development process.

  • Collaborate with creative services to ensure that revisions and appropriate changes are addressed within the scope of the project.

  • Collaboration and Communication:

  • Work closely with cross-functional teams to ensure project success, communicating effectively with internal professional services, clients, and key opinion leaders.

  • Regularly interface with internal teams, clients, and faculty during meetings and project discussions.

  • Compliance and Review Process:

  • Support the preparation of materials for pharmaceutical promotional review processes, ensuring compliance with submission requirements.

  • Revise content as needed through its internal and external reviews during the project lifecycle, adhering to medical/legal/regulatory (MLR) review process requirements.

  • Medical Event Attendance:

  • Attend live events such as professional conferences, advisory boards, and video productions to capture key content for project deliverables.

  • Produce high-quality editorial materials, such as executive summaries, articles, and presentations, based on event coverage.

  • Management and Mentorship:

  • Support and train direct reports to independently accomplish all essential roles and responsibilities described above. This will require supplying accurate precise directives for each assignment, review and guidance in best practices of writing/editing,

  • Provide training and mentorship to junior Medical Writers and Editors, offering guidance on best practices in medical writing and editing.

  • Assist in workload prioritization for your reports with deliverables and timelines of projects. ensuring timely delivery of high-quality content.

Qualifications:
  • Advanced degree (PharmD, DO, MD, MS, PhD) in a healthcare-related field (life sciences, biomedical sciences).

  • Minimum of 3 years experience in a medical communications agency or company, with specific experience in oncology.

  • Superior verbal and written communication skills.

  • Ability to multitask, manage multiple timelines, and solve problems effectively.

  • Proficiency in AMA style (11th edition) and in-house editorial standards.

  • Travel: Ability to travel for events, meetings, and video productions (3-5 days per month on average).

Compensation Range:
$90,000 - $100,000 per year, depending on qualifications. Eligible for annual company bonus program or commission incentive based on role. The compensation offered to the candidate selected for this position will depend on several factors, including the candidate's educational background, skills, and professional experience.
Benefits Overview:
We're proud to offer a comprehensive benefits package, including:
  • Hybrid work schedule
  • Health insurance through Cigna (medical & dental)
  • Vision coverage through VSP
  • Pharmacy benefits through OptumRx
  • FSA, HSA, Dependent Care FSA, and Limited Purpose FSA options
  • 401(k) and Roth 401(k) with company match
  • Pet discount program with PetAssure
  • Norton LifeLock identity theft protection
  • Employee Assistance Program (EAP) through NYLGBS
  • Fertility benefits through Progyny
  • Commuter benefits
  • Company-paid Short-Term and Long-Term Disability
  • Voluntary Term Life & AD&D Insurance, plus Universal Life Insurance options
  • Supplemental Aflac coverage: Accident, Critical Illness, and Hospital Indemnity
  • Discounts and rewards through BenefitHub

#LI-Remote
MJH Life Sciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. All employees of MJH Life Sciences are employed "At Will." This means that either the employee or the Company is free to end the employment relationship at any time, for any reason, with or without cause and with or without notice.

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