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Medical Writer Clinical Research Jobs (NOW HIRING)

$124 - $171/hr

## Medical Writer - Clinical ComplianceApplyremote type: Remotelocations: Remote-United Statestime type: Full timeposted on: Posted Yesterdayjob requisition id: R01132856Thank you for your interest in ...

Medical Writer

Boston, MA · On-site

$55 - $70/hr

Approximately 4+ years of relevant experience in medical writing, clinical research, drug development, or a related field. * Demonstrated experience writing and editing clinical and regulatory ...

Medical Writer - Clinical Compliance(Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of ...

Medical Writer - Clinical Compliance(Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of ...

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Medical Writer Clinical Research information

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$11

$46

$78

How much do medical writer clinical research jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical writer clinical research 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 writer clinical research?

A Medical Writer in Clinical Research is responsible for creating scientific documents related to clinical trials, regulatory submissions, and medical publications. They translate complex clinical data into clear, accurate, and compliant reports, protocols, and summaries. Medical Writers collaborate with researchers, regulatory teams, and healthcare professionals to ensure scientific integrity and compliance with industry standards. Strong writing skills, attention to detail, and knowledge of medical and regulatory guidelines are essential for this role.

What are the typical daily responsibilities of a medical writer clinical research?

As a Medical Writer in clinical research, your daily responsibilities often include drafting and editing clinical study protocols, investigator brochures, informed consent forms, and regulatory submissions such as clinical study reports (CSRs). You will collaborate closely with clinical teams, regulatory affairs, biostatisticians, and subject matter experts to gather necessary data and ensure all documents are clear, accurate, and aligned with regulatory guidelines. Managing multiple projects with tight deadlines is common, making organization and adaptability important. Successful medical writers play a crucial role in ensuring high-quality clinical documentation, ultimately supporting the drug development process and regulatory approvals.

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

A Medical Writer Clinical Research needs a strong background in life sciences or related fields, excellent writing skills, and experience in clinical research processes. Familiarity with regulatory submission systems (such as CTD/eCTD), referencing tools, and certifications like AMWA or EMWA are often advantageous. Attention to detail, time management, and the ability to communicate complex information clearly are vital soft skills for this role. These abilities ensure accurate, compliant documentation that supports clinical team goals and meets stringent regulatory standards.

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What cities are hiring for Medical Writer Clinical Research jobs?

Cities with the most Medical Writer Clinical Research job openings:

What are the most commonly searched types of Medical Writer Clinical Research jobs?

The most popular types of Medical Writer Clinical Research jobs are:

Infographic showing various Medical Writer Clinical Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Medical Writer - Clinical Compliance

3mcompany

On-site

$124 - $171/hr

Other

Medical, Dental, Vision, Life, Retirement

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


Job description

## Medical Writer - Clinical ComplianceApplyremote type: Remotelocations: Remote-United Statestime type: Full timeposted on: Posted Yesterdayjob requisition id: R01132856Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.**Job Description:****Medical Writer - Clinical Compliance(Solventum)****3M Health Care is now Solventum****At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.****We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.****The Impact You’ll Make in this Role** As a **Medical Writer – Clinical Compliance** you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:* Authoring and coordinating Clinical Evaluation Plans and Clinical Evaluation Reports (CEPs/CERs), to support new product introductions and sustaining product activities in the Dental Solutions business unit.* Collaborating with cross-functional teams to collect, analyze, and assess clinical data in compliance with EU MDR and other global regulatory requirements.* Supporting internal and external audits as a subject matter expert in clinical evaluations.* Maintaining up-to-date clinical evaluations across the full lifecycle of medical devices.* Contributing to Summary of Safety and Clinical Performance (SSCP) reports and regulatory responses with guidance from manager/supervisor.**Your Skills and Expertise** To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:* Bachelor’s degree or higher from an accredited institution, preferably in a scientific or technical discipline (Biology, Chemistry, Biomedical Eng, etc.) AND five (5) years of experience in the medical device industry ANDIn addition to the above requirements, the following are also required:* Minimum of five (5) years of experience in medical writing or technical writing in a regulated industry, preferably aligned to EU MDR requirementsAdditional qualifications that could help you succeed even further in this role include:* Strong scientific writing and communication skills, with the ability to interpret and present clinical data* Dental experience in a private, public, government or military environment* Demonstrated experience working on cross-functional teams in a global or regulatory environment* Familiarity with SSCP authoring and Class III/implantable medical device regulations in the EU* Excellent attention to detail, time management, and organizational skills* Ability to manage multiple complex projects simultaneously.* Strategic thinking, critical thinking, reasoning, and interpretive skills* Proficiency in Microsoft Office applications (Excel, Teams, Word, PowerPoint) with strong analytical skills.* Experience utilizing AI technologies to optimize workflows, automate tasks, and enhance operational efficiency.**Work location:** Remote – United States**Travel:** May include up to 10% domestic**Relocation Assistance:** Not authorized**Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).****Supporting Your Well-being**Solventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.Applicable to US Applicants Only:The expected compensation range for this position is $124,000 - $170,500, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-Rewards Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of **@solventum.com**. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.**Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.****Solventum Global Terms of Use and Privacy Statement**Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.Please access the linked document by clicking here. Before submitting your application you will be asked to confirm your agreement with the terms. #J-18808-Ljbffr