Senior Medical Writer Remote (Regulatory/Clinical)
MMS Holdings Inc.
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 managing project timelines. Applicants should possess exceptional writing skills and a solid understanding of the pharmaceutical industry. The ideal background includes a degree in a relevant scientific field and experience in leading teams. This role is vital in supporting clinical research and regulatory submissions. #J-18808-Ljbffr
- ...Job Description Senior Medical Writer - Clinical Development \n \n Immix Biopharma, Inc. \n \n United States / Remote / LA, CA \n \n Our 3 Core Values \n \n Intelligence... ...preparing, reviewing, and editing regulatory documents required for submission to...Remote workSeniorRegulatoryOdd job
- ...MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical protocols and study reports. This role requires at least 3-5 years of regulatory writing experience in the pharmaceutical industry....Remote workSeniorRegulatory
- ...Perceptive is seeking a Senior Medical Writer to research, write, edit, and coordinate clinical documents for independent review. The role involves serving as a primary... ..., ensuring adherence to SOPs, templates, and regulatory guidelines (FDA/EMA/ICH-GCP). You will...Remote workSeniorRegulatory
- 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
- 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
$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- ...Syneos Health in Canada/US remote role seeks a Sponsor Dedicated Protocol Medical Writer II/Sr to lead medical writing deliverables across studies. You’ll coordinate multi-department activities, ensure regulatory compliance, and mentor junior writers. Responsibilities...Remote workSeniorRegulatory
- ...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... ...improvements while working in a remote environment. #J-18808-LjbffrRemote workSeniorRegulatory
$142k - $153k
...Veristat in the United States is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across... ...working with cross-functional teams. This role offers remote work options, a competitive salary range of $142K–...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 workSeniorRegulatory- ...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,...Remote workSeniorRegulatory
- ...Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for autoimmune diseases. We are seeking a Senior Manager, Medical Writer to provide regulatory medical writing support for development programs and to serve as...Remote workSeniorRegulatory
- ...a full-service CRO, seeks a Principal Medical Writer to lead regulatory and scientific writing for complex submissions. You will translate clinical data into regulatory documents, mentor... ...collaboration across multidisciplinary teams. Remote or hybrid in San Diego is supported,...Remote workSeniorRegulatory
$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 workSeniorRegulatoryHourly payContract work- ...Parexel is seeking a Medical Writer to develop and finalize clinical documents for regulatory submissions, ensuring adherence to FDA/EMA guidelines and client SOPs. The... ...to manage timelines and mentor junior writers. Remote work options available. #J-18808-LjbffrRemote workSeniorRegulatory
- ...TransPerfect is seeking an organized, motivated medical writer to join our remote US team. The senior writer will partner with Clinical Development, Operations, Biostatistics, Regulatory, and Program Management to prepare high-quality regulatory documents under tight...Remote workSeniorRegulatory
- ...leading foundational AI lab to find experienced senior medical writers who can help train their latest language model... ...tasks. We seek candidates with 5+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate, and refine AI-generated...Remote workSeniorRegulatory
- ...Ethos is seeking senior medical writers with 5+ years in clinical research to help train an AI language model on professional... ..., and slide decks. This fully remote role offers 5-20 hours per week... ..., investigator brochures, and regulatory materials. Candidates must...Remote workSeniorRegulatoryImmediate startFlexible hours
- ...MMS, a data-focused clinical research organization, seeks an experienced Medical Writer to join a remote, globally oriented team. You will critically evaluate literature,... ...and study reports, and ensure high-quality regulatory submissions. The role emphasizes timely delivery...Remote workSeniorRegulatory
- ...operating company, in Irvine, CA, seeks a Senior Medical Writer to develop CERs and PMS reports for EU MDR and global regulatory standards. You will design literature searches... ...and collaborate across Scientific Affairs, Clinical Research, Regulatory Affairs, Engineering...SeniorRegulatory
- ...BeOne Medicines Ltd. is seeking a Senior Medical Writer to lead the creation, editing, and formatting of clinical regulatory documents in line with regulatory standards. The role requires collaboration across teams to ensure timely delivery and adherence to BeOne guidelines...SeniorRegulatory
- ...development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will take ownership of... ...cross-functional teams in a remote environment. Key... ...investigator brochures, and regulatory submissions Collaborate with...Remote workSeniorRegulatoryFull time
- ...TransPerfect is seeking an organized medical writer to lead planning and preparation of high-quality regulatory documents for clinical development. You will collaborate with Clinical... ...within timelines. The role is fully remote in the United States with on-site meetings...Remote workSeniorRegulatory
- ...Unknown company is seeking a Senior Medical Writer for remote US-based work. The role focuses on developing high-quality clinical and regulatory documents to support global submissions and regulatory compliance. You will coordinate with internal and external writers...Remote workSeniorRegulatory
- ...Parexel is seeking a Medical Writer in the United States to author and revise clinical documents for regulatory submissions. The role requires strong writing/editing skills, adherence to regulatory guidelines, and collaboration with cross-functional teams on project timelines...Remote workSeniorRegulatory
- ...kozmetickesluzby.vecnakraska.sk - Jobboard is looking for a Senior Medical Writer to work remotely in Rockford, IL. The role requires a strong background in regulatory and clinical medical writing, with at least 3-5 years of experience in the pharmaceutical industry....Remote workSeniorRegulatory
- ...MMS, a data-focused clinical research organization, seeks a Medical Writer to craft regulatory and clinical development documents. You will work with cross-functional teams... ...authoring projects under tight deadlines. Remote work is available for Brazil-based candidates....Remote workSeniorRegulatory
- ...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 workSeniorRegulatoryWork from home
- A dynamic company in healthcare is seeking an experienced Medical Writer to lead the development of clinical and regulatory documents. This role involves drafting, editing, and managing submissions while collaborating with cross-functional teams. Candidates should have...SeniorRegulatory
- ...ACM Global Laboratories, Inc. is seeking a Medical Writer to interpret complex clinical study protocols and prepare study-specific medical and technical... ...with multiple departments to ensure accuracy and regulatory compliance. Responsibilities include leading document...Remote workRegulatory
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