Senior Medical Writer — Remote Regulatory Lead
Itlearn360
- Remote job
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 in neuromuscular or rare diseases, and strong project management skills. This position offers a temporary contract with potential for extension and competitive hourly compensation. #J-18808-Ljbffr Itlearn360
$89k - $148k
A leading healthcare company is seeking an experienced medical writer to lead projects for Clinical Research Scientists and other... ...complex research into regulatory documents and mentoring team members... ..., plus bonuses, with the potential for remote work. #J-18808-LjbffrRemote workSeniorRegulatory- ...Johnson in the United States is seeking a Regulatory Medical Writer to support Immunology programs within... ...2 days from home, with case-by-case remote options. You will write and coordinate... ...(CSRs, IBs, protocols, RMPs), lead cross-functional planning, establish timelines...Remote workSeniorRegulatory
- 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 of medical... ...exceptional communication and regulatory knowledge. Competitive salary and...Remote jobSeniorRegulatoryFixed term contract
- 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
- ...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
- ...Leading the development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will manage the preparation and review... ...flexibility to work remotely or onsite. Key... ...biostatistics, and regulatory affairs to analyze...Remote workSeniorRegulatoryFull time
$70 - $80 per hour
...firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function... ...drafting clinical study protocols, regulatory documents, and managing review timelines... ...This full-time position is primarily remote, with a competitive pay range of $70 -...Remote workSeniorRegulatoryHourly payFull timeContract work$116k - $128k
...Strategies, LLC is looking for a Senior Medical Writer specializing in clinical... .... This role involves leading document authorship, interfacing... ...degree and over 3 years of regulatory writing experience. A... ...various benefits including remote work options and medical insurance...Remote workSeniorRegulatory$50 - $80 per hour
...YO AI Labs seeks an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory... ..., and high-quality medical writing. This remote contractor role offers an hourly pay rate...Remote workSeniorRegulatoryHourly payFor contractors- ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents... ..., Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP)...Remote workSeniorRegulatory
- ...400670Reference26-00910Remote50% Remote Job Description Key Responsibilities · Lead FDA audit and inspection readiness... .../interface for FDA inspections, regulatory meetings, and compliance discussions... ...industries such as Pharma, Medical Devices, Biotechnology, or Healthcare...Remote workSeniorRegulatory
- ...Senior Medical Writer Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation The Senior Medical Writer provides... ...use of software for document development, document types, regulatory requirements, and therapeutic area knowledge. Ensure...Remote workSeniorRegulatoryContract work
- ...Medical Writer MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech... ...approach to complex trial data and regulatory submission challenges. With a global... ...clinical study protocol experience, as lead author, required Experience leading...Remote workSeniorRegulatoryWorldwide
- ...Senior Medical Writer When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide...Remote workSeniorRegulatory
- ...Senior Medical Writer Join us as we transform immunology and deliver medicines that help autoimmune... ...nonclinical, and safety documents for regulatory submissions. This individual will... ...writing activities Supports the lead writer and project teams to ensure project...Remote workSeniorRegulatory
- ...Senior Medical Writer This position is listed on behalf of a partner company... ...Brazil. This is a fully remote opportunity for an experienced... ...to clinical development and regulatory submission projects. You... ...Contribute substantially to, or lead, the development of...Remote workSeniorRegulatoryFull time
$95k - $125k
...Senior Medical Writer, Medical Communications Remote, United States Are you passionate about transforming complex... ...strategic storytelling, partnering with leading pharmaceutical and biotech... ...across therapeutic areas, regulatory standards, and key statistical concepts...Remote workSeniorRegulatory- ...Clinical Regulatory Document Specialist Company Overview Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in...Remote workSeniorRegulatoryInterim roleWorldwide
- ...Senior Medical Writer Synterex, Inc. is a global consortium of highly experienced... ...operations support. Synterex offers remote or on-site services, with a... ...Clinical Operations, Biostatistics, Regulatory, and Program Management in leading the planning and preparation of...Remote workSeniorRegulatoryLocal area
$85k - $100k
...Join to apply for the Senior Medical Writer role at Flywheel Partners . Flywheel... ...agency that supports leading healthcare companies by developing... ..., Sales, Legal, and Regulatory stakeholders. Build rapport... ...communication, and workload in a remote setting. Salary Range: $85K...Remote workSeniorRegulatory$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory teams to produce a range of medical documents for regulatory submissions, including clinical evaluation reports and study protocols...Remote jobSeniorRegulatory- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents... ..., and mentoring team members. A strong background in regulatory writing and at least 3 years of experience in the pharmaceutical...Remote jobSeniorRegulatory
$120k - $159k
...Indegene Company, is hiring Senior/Principal Medical Writers (USA) to support our growing company in producing regulatory documentation for the... ...time); may work either fully remotely or a hybrid schedule (in office... ...publications) as the lead writer in collaboration with...Remote workSeniorRegulatoryLive inWork at officeWork visa- ...Senior Medical Writer At GSK, we have bold ambitions for patients, aiming... ...clinical documents, including regulatory documents following defined... ...within GSK (e.g., Clinical Leads, Asset Leads, Study Delivery... ...collaboration and use flexible remote working for focused writing....Remote workSeniorRegulatoryWork at officeLocal areaFlexible hours
$128.6k - $210k
...Senior Medical Writer At Regeneron, we use science and innovation to develop life-changing medicines... ...across Global Development in a remote work mode. In this role, you will author... ...narratives, investigator brochures, and other regulatory documents across therapeutic areas....Remote workSeniorRegulatoryWorldwide- ...biopharmaceutical solutions company is seeking a Sr Medical Writer to lead medical writing deliverables and ensure compliance with regulatory standards. Responsibilities include... ...writing and ICH guidelines. The role is remote-based and offers competitive benefits such...Remote jobSeniorRegulatoryFlexible hours
- Parexel is seeking a Medical Writer to develop and finalize clinical documents for regulatory submissions, including study reports, protocols, and CTD overviews. You will... ...with FDA/EMA guidelines. The role involves leading document development on projects, coordinating...Remote jobSeniorRegulatory
- ...Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical research organisation... ...Medical Writer at ICON, you will lead the development and execution of... ..., investigator brochures (IBs), and regulatory submissions, ensuring accuracy,...Remote workSeniorRegulatory
- Axle is seeking a Senior Medical Writer & Regulatory Affairs Consultant to support the NIH Blueprint Neurotherapeutics Network (BPN) at NIH in Rockville, MD. This role provides scientific leadership and regulatory expertise throughout drug discovery and development by...SeniorRegulatory
- ...Senior Medical Writer- ICON- Remote USA ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive... ...reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity...Remote workSeniorRegulatoryFlexible hours
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