Senior Medical Writer — Remote (Regulatory/Clinical)
MMS Holdings Inc
- 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 in the pharmaceutical industry is essential. Ideal candidates will also hold a relevant degree and possess exceptional writing and organizational skills. #J-18808-Ljbffr MMS Holdings Inc
$116k - $128k
...Strategies, LLC is looking for a Senior Medical Writer specializing in clinical documentation. This role involves... ...Bachelor's degree and over 3 years of regulatory writing experience. A strong... ..., with various benefits including remote work options and medical insurance...Remote workSeniorRegulatory- ...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 closely with clients...Remote jobSeniorRegulatory
- 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 jobSeniorRegulatory
- 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 jobSeniorRegulatory
- ...Syneos Health is seeking a Principal / Senior Medical Writer with proven clinical document writing experience. This remote role supports global regulatory deliverables and cross-functional collaboration across study teams and clients. Ideal candidates bring extensive experience...Remote workSeniorRegulatory
- ...development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will manage the... ...the flexibility to work remotely or onsite. Key responsibilities... ...research, biostatistics, and regulatory affairs to analyze...Remote workSeniorRegulatoryFull time
$70 - $80 per hour
...specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review... ...This full-time position is primarily remote, with a competitive pay range of $...Remote workSeniorRegulatoryHourly payFull timeContract work- A clinical-stage biotechnology company is seeking a Medical Writer to lead the development of regulatory and clinical documents. The role requires expertise in medical writing and collaboration with various teams to ensure high-quality documentation. Candidates should...SeniorRegulatory
- ...pharmaceutical, biotech, and medical device industries with a proven... ...to complex trial data and regulatory submission challenges. With a... ...minimal supervision, the Medical Writer will critically evaluate,... ...absence of bias Write and edit clinical development documents,...Remote workSeniorRegulatoryWorldwide
$85k - $100k
...Join to apply for the Senior Medical Writer role at Flywheel Partners . Flywheel... ...workshops—to enhance clinical dialogue with healthcare providers... ..., Sales, Legal, and Regulatory stakeholders. Build rapport... ...communication, and workload in a remote setting. Salary Range: $85K...Remote workSeniorRegulatory- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses... ...scientific information into regulatory-ready documents. Candidates... ...encouraged to apply. This is a remote role with an initial contract...Remote workRegulatoryContract work
$120k - $159k
...Indegene Company, is hiring Senior/Principal Medical Writers (USA) to support our growing company in producing regulatory documentation for the... ...writers are integral members of clinical development teams... ...time); may work either fully remotely or a hybrid schedule (in office...Remote workSeniorRegulatoryLive inWork at officeWork visa- ...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...Remote workRegulatoryContract work
- ...of highly experienced clinical development professionals specializing in medical writing, submission... ...support. Synterex offers remote or on-site services,... ...writing team. The senior medical writer will partner cross-functionally... ..., Biostatistics, Regulatory, and Program...Remote workSeniorRegulatoryLocal area
- ...has an exciting opportunity for a Medical Writer ! Key Accountabilities Author Clinical Documents Gather, review,... ...clinical documents for submission to regulatory authorities, including but not... ...or equivalent. #LI-KW1 #LI-REMOTE EEO Disclaimer Parexel is an...Remote workSeniorRegulatoryInterim roleFlexible hours
$55 - $75 per hour
...with significant unmet medical need. We enlist the... ...pipeline of commercial, clinical and preclinical... ...is a Contract role- Remote can live anywhere in... ...55 to $75hour The Senior Medical Writer applies advanced documentation... ...study results for regulatory submissions and...Remote workSeniorRegulatoryFull timeContract workFor contractorsWorldwideShift work$89k - $148k
...company is seeking an experienced medical writer to lead projects for Clinical Research Scientists and other stakeholders... ...complex research into regulatory documents and mentoring team members... ...annually, plus bonuses, with the potential for remote work. #J-18808-LjbffrRemote workSeniorRegulatory$110k - $125k
...Description We are excited to expand our Medical Writing FSP Team and are seeking candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you will... ...a proven track record in authoring clinical regulatory documents; ideally they will also bring...Remote workSeniorRegulatoryFull timeTemporary work- INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home based anywhere in the US. The ideal candidate will mentor junior writers while managing complex medical writing tasks across various therapeutic...Remote jobSeniorRegulatoryWork from home
- ...A leading global clinical research organization is seeking a Senior Medical Writer I for a 12-month FTC, fully remote. In this role, you will spearhead the development and execution... ...possess exceptional communication and regulatory knowledge. Competitive salary and...Remote workSeniorRegulatoryFixed term contract
- Senior Medical Writer I 12 Months FTC I Fully Remote I Based in EU A leading global clinical research organization is seeking a Senior or Principal Medical Writer to join its... ...CSRs), investigator brochures (IBs), and regulatory submission documents. Collaborate with cross...Remote workSeniorRegulatoryFixed term contract
- ...Itlearn360 is seeking a Senior Medical Writer in South San Francisco. This role involves overseeing high-quality documents for clinical trials and regulatory submissions. The ideal candidate should have 8-10 years of scientific writing experience, including expertise...Remote workSeniorRegulatoryHourly payTemporary work
$50 - $80 per hour
...Job Description Job Description Job Title: Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50–$80/hour... ...Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory...Remote jobRegulatoryFor contractors$90k - $100k
...Experience . Position Summary The Senior Medical Writer serves as an integral part... ...compelling and relevant clinical communications and... ...Lambertville, or San Francisco—or remotely within the US, depending on... ...for client medical/legal/regulatory reviews by highlighting all...Remote workSeniorRegulatoryWork experience placementCasual workWork at officeLocal areaNight shiftWeekend work2 days per week- ...NAMSA, a premier MedTech development partner, seeks a Clinical Research Associate to monitor sites and ensure GCP and regulatory compliance across assigned studies. You will coordinate on-site and remote visits, track enrollment, and maintain study documentation to support...Remote workSeniorRegulatory
- ...A leading organization in clinical research is seeking a Clinical Research Associate to ensure that clinical studies are conducted in compliance with regulatory requirements. The role involves significant travel, monitoring clinical sites, and maintaining robust documentation...Remote workSeniorRegulatory
- ...AnnuallyIndustry PharmaceuticalsSelling Points Drive clinical quality excellence in a hybrid executive role. Lead impactful audits and regulatory initiatives for compliance success.... ...corrective action plans.Supervise remote vendor audits, ensuring thorough follow-up...Remote workSeniorRegulatory
- ...A leading clinical research organization is seeking a Senior Project Manager to oversee and execute clinical trials. This fully remote position requires strong project management skills, relevant... ...while ensuring compliance with regulatory standards. #J-18808-Ljbffr...Remote workSeniorRegulatory
- ...Worldwide Clinical Trials seeks a Senior Clinical Research Associate (CNS) to support Midwest and Southeast regions with remote options. You will lead site management across CNS studies, coordinating regulatory docs, budgets, and data capture while ensuring patient safety...Remote workSeniorRegulatoryWorldwide
- ...the operational delivery of one or more cell therapy clinical trials, the full-time remote Senior Clinical Trial Manager will oversee study design through... ...and vendor oversight while ensuring compliance with regulatory standards. Key responsibilities Manage the day-to-...Remote workSeniorRegulatoryFull time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Medical Writer — Remote (Regulatory/Clinical). Be the first to apply!
- senior safety specialist Denver, CO
- senior technology project manager Denver, CO
- remote senior business analyst Denver, CO
- senior manager clinical operations Denver, CO
- senior supervisor Denver, CO
- senior leadership Denver, CO
- senior manager data science Denver, CO
- senior business analyst Denver, CO
- senior relationship manager Denver, CO
- senior director engineering Denver, CO



