Medical Writer - Clinical Compliance
$124k - $170.5kSOLVENTUM
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
AND
In 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 requirements
Additional 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: 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.
- ...Working remotely as a contract Clinical Medical Writer, the candidate will develop high-quality regulatory documents for submission to Sponsors and regulatory agencies, ensuring compliance and scientific rigor. Key responsibilities: Lead the planning, development, and...SuggestedContract workRemote work
- ...To support clinical research initiatives, the full-time remote Medical Writer will author clinical trial and regulatory documents, engage with cross-functional teams, and ensure document quality and compliance. Key responsibilities Author clinical trial and regulatory...SuggestedFull timeRemote work
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses on drafting a Clinical Development Plan and protocols for early feasibility studies. Candidates should have experience with medical device...SuggestedContract workRemote work
- ...Sr Medical Writer Publications - Sponsor Dedicated - Remote Based Syneos Health is a leading... ...customer success. We translate unique clinical, medical affairs and commercial... ...employees. The Company is committed to compliance with the Americans with Disabilities Act...SuggestedContract workRemote workFlexible hours
$116k - $128k
...Synchrogenix Information Strategies, LLC is looking for a Senior Medical Writer specializing in clinical documentation. This role involves leading document authorship, interfacing directly with clients, and supporting comprehensive projects within a collaborative team...SuggestedRemote work$40 - $47 per hour
...Job Summary Our client is seeking a Medical Affairs Writer to support the department in coordinating medical training and compliance-related tasks. The role provides group support... ...leaders, healthcare providers, vendors, clinical study sites, advisory boards, and others....Hourly payWork experience placementWork at officeLocal areaRemote work- ...Holdings Inc in Austin, Texas seeks a skilled Medical Writer to evaluate medical literature and write essential clinical documents. Candidates should have 3-5 years of... ...timelines and mentoring team members while ensuring compliance with rigorous standards. Exceptional writing...Remote job
- Celerion is seeking a Medical Writer to work remotely. The role analyzes and interprets safety results from clinical trials, compiling, writing and editing clinical study reports... ...scientific reports while ensuring compliance with GCP/ICH and client specifications....Remote job
- MMS Holdings Inc, based in Michigan, is seeking an experienced Medical Writer to take on critical analysis and writing responsibilities for clinical development documents. The ideal candidate will have 3-5 years of experience in regulatory writing and anticipate working...Remote job
- Parexel is seeking a Medical Writer to develop and finalize clinical documents for regulatory submissions, including study reports, protocols, and CTD overviews. You will ensure accuracy, consistency, and alignment with FDA/EMA guidelines. The role involves leading document...Remote job
- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents, evaluating medical literature, and mentoring team members. A strong background in regulatory writing and at least 3 years of experience...Remote job
- MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and...Remote job
- MMS Holdings Inc in Baltimore, Maryland is seeking a Medical Writer to critically evaluate and write clinical documents for regulatory submissions. This role demands experience in the pharmaceutical industry and exceptional writing skills to produce high-quality documentation...Remote job
- Celerion is seeking a Medical Writer to work remotely. The role analyzes and interprets safety results of clinical trials, compiles, writes and edits CSR and other industry documents, and confirms accurate classification of events using standardized coding systems. The...Remote job
- ...biopharmaceutical solutions company is seeking a Sr Medical Writer to lead medical writing deliverables and ensure compliance with regulatory standards. Responsibilities include managing writing activities for clinical studies, completing diverse documents, and...Remote jobFlexible hours
$71.25k - $101.78k
Payfuture Technologies is seeking a Medical Writer for DynaMedex. This remote/hybrid role requires strong writing skills for medical content... ...relevant experience are essential for success in summarizing clinical evidence. The position offers a competitive salary ranging...Remote job- ...To support quality improvement initiatives, the full-time Arizona Licensed Clinical Data Abstractor will abstract and audit complex clinical data remotely, ensuring compliance with care standards while maintaining established productivity and accuracy. Key responsibilities...Full timeRemote work
- Precision Medicine Group seeks a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents with high quality and on-time delivery... ..., IBs, ICFs, DSURs, and CSRs while ensuring compliance with ICH, FDA, GCP, and eCTD standards. The candidate...Remote job
- ...Job Summary: Located at Temperance at Lake Ridge The Clinical Administrative Assistant / Residential Care Coordinator provides... ...coordinates resident care needs, maintains staff schedules, supports compliance with state regulations, and assists with on-call...Full timeWork at officeLocal areaAll shiftsMonday to FridayWeekend workAfternoon shift
- ...Downtown Evansville Inc. is seeking a Clinical Documentation Improvement Specialist - RN... ...Evansville, IN. The CDI Specialist will review medical records, identify missing or vague... ...and coordinate with Coding, Quality and Compliance to improve documentation accuracy. Requirements...Remote work
- ...primarily in a remote environment, the full-time Clinical Documentation Improvement Specialist will review medical records to ensure accurate documentation of... ...professionals to enhance documentation quality and compliance. Key responsibilities Review medical records for...Full timeRemote work
- ...enhance the quality and completeness of clinical documentation, the full-time remote Clinical... ...with healthcare providers, assess medical records, and implement documentation improvement strategies while ensuring compliance with healthcare regulations. Key responsibilities...Full timeRemote work
$96k - $132k
...Clinical Documentation Specialist (CDI) (Solventum) At Solventum, we enable better, smarter, safer... ...concurrent and/or retrospective reviews of inpatient medical records for documentation accuracy, completeness, and compliance. Maintain an accuracy rate of 98%...H1bWork at officeRemote workRelocation packageFlexible hours- ...Performing clinical claim reviews, the part-time Massachusetts Licensed Clinical Review... ...accuracy and charge correctness, ensuring compliance with state and federal guidelines while... ...Conduct clinical reviews of claims against medical records to assess support for claims...Part timeWork at officeRemote work
- ...Clinical Quality Reviewer Ensures compliance with the contract, and program requirements for Clinical Quality Management (CQM) within West Region. To... ...beneficiaries by identifying, investigating, and evaluating medical records retrospectively for potential quality, safety...Contract workInterim roleRemote work
- Medical Writer (Consultant) - Clinical Development / Early Feasibility Study Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates residing in Europe are also encouraged to apply. Overview We are seeking an experienced Medical Writer to support the initial...Contract workImmediate startRemote work
- ...Clinical Documentation Specialist Under the direction of CDI Manager, the Clinical Documentation Specialist reviews medical records to facilitate accurate and complete medical record documentation... ...and procedural information for compliance to CMS, DOH regulatory, and...Remote workWork from home
- Adventist HealthCare in Maryland is hiring a Clinical Documentation Specialist to enhance accuracy of patient records, ensure compliance with CMS guidelines, and support accurate ICD-10-CM/PCS and CPT coding. The role involves collaborating with physicians and care teams...Remote job
$70k - $120k
...Fully Remote: Clinical Documentation Specialist Facilitate the improvement of clinical... ...concurrent and retrospective reviews of medical records to ensure accurate documentation... ...opportunities for documentation improvement. Ensure compliance with regulatory requirements and...Local areaRemote workMonday to Friday- ...Leads the clear and accurate completion of medical writing deliverables, ensuring... ...Mentors and leads less experienced medical writers on complex projects, as necessary. Develops... .... The Company is committed to compliance with the Americans with Disabilities Act...Remote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Writer - Clinical Compliance. Be the first to apply!


