Medical Writer: Clinical Dev & EFS (Remote)
Confidential
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 studies and be able to convert complex scientific information into regulatory-ready documents. Candidates based in the U.S. and Europe are encouraged to apply. This is a remote role with an initial contract of 6-12 months. #J-18808-Ljbffr
- 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... ...with Early Feasibility Studies (EFS) and/or First-in-Human trials IND or...Remote workContract workImmediate start
$50 - $80 per hour
...Job Description Job Description Job Title: Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50–$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and...Remote workFor contractors$50 - $80 per hour
...Role Overview Apply regulatory medical writing expertise to author and evaluate clinical documentation used to train and assess AI-assisted writing tools. In... ...Terms Engagement type: Contractor. Location: Remote. Project focus: Contributing to a client project...Remote workHourly 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, and mentoring team members. A strong background in regulatory writing and at least 3 years of experience...Remote job
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division, remotely anywhere in the United States. The role focuses on developing regulatory and clinical documentation to support global registrations and lifecycle management, partnering with Regulatory,...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 and other industry documents. It requires accurate classification of events and medications...Remote job
- Crossing Hurdles is seeking a Medical Writer / Clinical Document Author on a contract basis to support AI tool development. This remote role requires strong regulatory medical writing experience and the ability to author or lead full Clinical Study Reports. You will review...Remote jobContract work
- 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
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division. This role is based remotely within the United States, collaborating with Regulatory Affairs, Clinical Affairs, Quality, R&D, and Marketing to translate complex clinical data into regulatory and...Remote job
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents... ...compliance, and high-quality medical writing. This is a remote contractor role requiring strong writing and cross-functional...Remote jobFor 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 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
- 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
- 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. The role emphasizes planning, writing, editing, formatting, and QC across protocols, IBs, ICFs, DSURs,...Remote job
- YO AI Labs seeks Medical Evaluation Specialists to craft and validate challenging medical... ...questions for evaluating AI systems. This remote contractor role welcomes medical students... ...with citations, and assess AI outputs for clinical accuracy and reasoning. Medical knowledge...Remote workFor contractors
$165k - $185k
...skills (Clinician's Brief), clinical and pharmaceutical decision support... ...Your Role This is a fully remote role. Are you a boarded... ...of Care team as a full-time writer. In this unique role, you'll... ...experience. ~ Proven experience in medical content development and...Remote workFull time- ...Medical Writer / Clinical Document Author is a remote clinical-review track for evaluating AI outputs that touch clinical review. Reviewers grade differential reasoning, dosing logic, and guideline adherence; flag patient-safety issues; and document the corrected clinical...Remote jobHourly payFor contractors10 hours per week
$50 - $80 per hour
...Role Overview Apply regulatory medical writing expertise to author and evaluate clinical documentation that trains and validates AI-assisted clinical writing... ...priority. Work Terms Engagement type, contractor, remote work. Work is performed on a customer project...Remote workHourly payContract workFor contractorsLocal area- ...development. Competitive Compensation: ~ Medical/Dental ~ Generous Paid Time Off ~401K... ...their needs and desires. Outpatient Clinical Documentation Integrity Specialist JOB... ..., audits, and follow-up activities in a remote environment. Strives to Exceed...Remote workLocal areaFlexible hours
- ...Working remotely in a full-time capacity, the Medical Writer will analyze and interpret safety results from clinical trials, compile and write clinical study reports, and ensure compliance with regulatory standards. Key responsibilities Analyze and interpret various...Remote workFull time
- ...MMS Holdings Inc is seeking an experienced Medical Writer located in Bridgeport, Connecticut, to support the pharmaceutical and biotech industries. The role involves writing clinical development documents and requires a strong background in regulatory writing alongside...Remote work
- ...Cabaletta Bio is seeking a Manager, Medical Writer and Quality Control Specialist for remote work to support regulatory affairs and clinical development. This role partners with clinical and regulatory teams to produce high-quality documentation for regulators, editors...Remote work
- ...YO AI Labs seeks an experienced Medical Writer/Clinical Document Author to develop, review, and evaluate regulatory documents, ensuring scientific... ...collaborate with cross-functional teams to drive quality. Remote-friendly environment with emphasis on precision and...Remote work
- ...YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents with a focus on scientific accuracy and regulatory compliance. The role emphasizes high-quality medical writing, CSR authoring...Remote work
- ...Syneos Health, Inc. is seeking a Sponsor Dedicated Protocol Medical Writer II/Sr for a remote-based role. You will lead the creation and review of... ...sites with mentorship to junior writers. You will work with clinical scientists, data management, and regulatory staff to...Remote work
- ...Stryker is hiring a Senior Staff Medical Writer for its Endoscopy Division. This remote, nationwide role focuses on developing regulatory and scientific documents... ...of medical devices. You will translate complex clinical evidence into CERs, PMCF, and other submissions,...Remote work
- ...Knowesis is seeking a Medical Writer in East Orange, NJ with remote work options to support the VA EXPRT Center. The role involves developing clinical and research documents, educational outreach, and quality assurance of materials for diverse audiences. Applicants should...Remote work
- ...Stryker is hiring a Senior Staff Medical Writer to join the Endoscopy Division. This remote role supports the US market for regulatory and scientific documentation... ...States, you will author CERs, PMCF, and other clinical evidence documents, synthesize data from studies and...Remote work
- ...Sumitomo Pharma is seeking a QC Medical Writer for a primarily remote role with occasional on-site meetings. You will perform QC audits of clinical regulatory documents, collaborate with the Medical Writing team, and help maintain AMA-style templates and SOPs. The role...Remote work
$145k - $155k
...Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote) Position Overview This is a Temp-To-Hire Position Primary contact for medical writing... ...typical job duties include: Collaborating with the clinical & regulatory teams to write clinical documents for...Remote workTemporary workInterim role
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