Senior Medical Writer Clinical Regulatory Expert (Remote)
$142k - $153kVeristat
- Remote job
Veristat in the United States is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across product development stages. You will organize, analyze, interpret, and present scientific and statistical information in line with ICH and company standards, working with cross-functional teams. This role offers remote work options, a competitive salary range of $142K–$153K USD plus bonus, and benefits such as medical insurance, tuition #J-18808-Ljbffr Veristat
- ...Senior Medical Writer - Clinical Development Immix Biopharma, Inc. United States / Remote / LA, CA Our 3 Core Values Intelligence... ..., reviewing, and editing regulatory documents required for submission... ...meetings and provide expert advice on regulatory...Remote workSeniorRegulatoryOdd jobFull time
$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 jobSeniorRegulatoryHourly payFor contractors- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents, evaluating medical literature,... ...mentoring team members. A strong background in regulatory writing and at least 3 years of experience...Remote jobSeniorRegulatory
- ESR Healthcare in New York, NY invites a Medical Writer (Pharmaceutical) to join as a contractor, focused on regulatory writing for AI-assisted clinical documentation. Remote work with NYC placement is offered, aiming for expert judgment across efficacy and safety narratives...Remote jobSeniorRegulatoryFor contractors
- MMS 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 regulatory writing experience within the pharmaceutical industry. The Medical Writer is responsible...Remote jobSeniorRegulatory
- ...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
- micro1 is seeking Medical Writers / Clinical Document Authors to participate in a customer project focused on developing AI... ...writing tools for clinical documentation. In this remote contractor role, you will apply regulatory expertise to train AI systems and shape how...Remote jobSeniorRegulatoryFor contractors
- Syneos Health, Inc. is seeking a Senior Medical Writer (FSP) with proven experience in clinical document writing, including... ...IBs. The role emphasizes meeting regulatory standards while delivering high... ...schedule. The position supports remote work with flexibility across...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
- ...focused CRO, is seeking an experienced Medical Writer to critically assess literature, craft clinical development documents, and manage writing projects for regulatory submissions. The role requires... ...writing, advanced degrees, and expert MS Word/Office skills, with a...Remote jobSeniorRegulatory
$80.6k - $175.7k
Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs) Updated: Today Location: Remote, MO, United States Job ID: 25112637 Description Senior Medical Writer... ...meetings. Adheres to established regulatory standards, including, but not...Remote workSeniorRegulatoryContract workFlexible hours- Perceptive is seeking a Senior Medical Writer to create, edit, and coordinate clinical documents for independent review and regulatory submissions. The role involves serving as a key client... ...teams in a fast-paced, fully remote US environment. #J-18808-Ljbffr PerceptiveRemote jobSeniorRegulatory
- ...leading healthcare intelligence and clinical research organization, is seeking a Senior Principal Medical Writer to lead development of high-quality clinical and regulatory documents. The role requires... ...while working in a remote environment. #J-18808-Ljbffr Sal...Remote jobSeniorRegulatory
- ...Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech... ...• Partner cross-functionally with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear,...Remote workSeniorRegulatoryWork at office
$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... ...trial data and regulatory submission challenges.... ...supervision, the Medical Writer will critically... ...bias Write and edit clinical development documents,... ...regulatory documents Expert proficiency with client...Remote workSeniorRegulatoryWorldwide
- ...Job Title Provides high-quality regulatory medical and scientific writing in support of Phase 1–3 clinical development of pharmaceutical and biologic products, from... ...documents. Reviews documents prepared by junior writers and peers. May provide training and mentorship...Remote workSeniorRegulatoryContract work
- ...individual for our medical writing team. The senior medical writer will partner cross... ...client teams in Clinical Development, Clinical... ..., Biostatistics, Regulatory, and Program... ...Location: Fully remote in the US, but must... ...documents Serve as an expert on client document...Remote workSeniorRegulatoryLocal area
$85k - $100k
...Join to apply for the Senior Medical Writer role at Flywheel... ...workshops—to enhance clinical dialogue with healthcare... ...owners and subject‑matter experts to create engaging... ..., Sales, Legal, and Regulatory stakeholders. Build rapport... ..., and workload in a remote setting. Salary Range...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
$78k - $156k
...leading businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...currently has an on-site opportunity for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical...SeniorRegulatoryWork experience placementWorldwideShift work- .... is seeking a Sponsor Dedicated Protocol Medical Writer II/Sr for US/Canada remote work. The role involves partnering with Clinical Scientists and leading medical writing deliverables... ...supervision and ensure adherence to regulatory standards. The position requires 3-5 years...Remote jobSeniorRegulatory
- ...Environmental Conditions Office Job Description Senior Regulatory Medical Writer (FSP; Remote; US) At Thermo Fisher Scientific, you will discover... ..., and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development...Remote workSeniorRegulatoryWork at officeLocal areaFlexible hoursDay shift
- SimulStat Inc. seeks a Sr. Medical Writer to support the development of global regulatory documentation strategy and the execution of tactics. You will conceptualize... ...medical communications for reviewer-friendly clinical documents to support regulatory agency review, coordinating...Remote jobSeniorRegulatory
- Thermo Fisher Scientific is seeking a Senior Regulatory Medical Writer for a flexible, remote US role within the FSP team. You will author clinical regulatory documents from planning to delivery, collaborating with clients and internal teams to ensure accuracy and regulatory...Remote jobSeniorRegulatoryFlexible hours
$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- A global medical device consulting firm is looking for a EUMDR Medical Writer for a remote, full-time engagement. Candidates should have a... ...full benefits and focuses on clinical documentation, literature reviews, and compliance with regulatory guidelines. Strong written...Remote jobRegulatoryFull time
$55 - $75 per hour
A leader in biotechnology is seeking a Senior Medical Writer to draft and manage clinical documentation. This remote contract position offers a competitive hourly rate... ...writing skills, and a deep understanding of regulatory requirements. This role is crucial in supporting...Remote jobSeniorRegulatoryHourly payContract work$84.37k - $120.53k
## Senior Medical WriterApply: Remote (US): Full time: Posted 2 Days Ago: JR104959**About... ...is to shape the future of clinical research. With decades of... ...role**A Senior Medical Writer will create, research, edit... ...documents for submission to regulatory authorities.* Prepare,...Remote workSeniorRegulatoryFull timeContract workWork at officeFlexible hours
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