Senior Medical Writer — Remote (Regulatory/Clinical)
MMS Holdings Inc
- 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 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 MMS Holdings Inc
$116k - $128k
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$70 - $80 per hour
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...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- ...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
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$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$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
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$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
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- ...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
- ...biotechnology company is looking for a Senior Clinical Research Associate to oversee clinical... ...responsibilities including site management, regulatory compliance, and data quality assurance.... ...multiple sites effectively. This remote role offers an opportunity to significantly...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
- ...Health, Inc. is seeking a CRA II/Sr CRA for remote work based in Germany. This role... ...management tasks, ensuring compliance with regulatory standards, and liaising with site personnel... ...field, fluency in German, and prior clinical monitoring experience in Germany. You will...Remote workSeniorRegulatory
- ...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
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