Senior Medical Writer — Remote (Regulatory/Clinical)
MMS Holdings Inc
Denver, CO
- Remote job
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 in the pharmaceutical industry is essential. Ideal candidates will also hold a relevant degree and possess exceptional writing and organizational skills. #J-18808-Ljbffr MMS Holdings Inc
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Senior Medical Writer — Remote (Regulatory/Clinical) in Denver, CO vacancy
- ...Holdings Inc is looking for a skilled Medical Writer to join their team in Atlanta, Georgia.... ...minimum of 3-5 years of experience in regulatory writing within the pharmaceutical industry... ...medical literature, writing various clinical documents, and mentoring junior writers...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
- 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
- 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 jobSeniorRegulatory
$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 workTalent Software Services
United States4 days ago- ...pharmaceutical, biotech, and medical device industries with a proven... ...to complex trial data and regulatory submission challenges. With a... ...minimal supervision, the Medical Writer will critically evaluate,... ...absence of bias Write and edit clinical development documents,...Remote workSeniorRegulatoryWorldwide
MMS
Bridgeport, CT1 day ago - ...Summarized Purpose: Provides high-quality regulatory medical and scientific writing in support of Phase 1-3 clinical development of pharmaceutical and biologic... ...documents. Reviews documents prepared by junior writers and peers. May provide training and...Remote workSeniorRegulatoryContract work
Katalyst Healthcares and Life Sciences
United States19 hours ago - ...collaborative individual for our medical writing team. The senior medical writer will partner cross-... ...with client teams in Clinical Development, Clinical... ..., Biostatistics, Regulatory, and Program Management... ...Location: Fully remote in the US, but must be...Remote workSeniorRegulatoryLocal area
TransPerfect
United States4 days ago - ...of highly experienced clinical development professionals specializing in medical writing, submission publishing... ...support.Synterexoffers remote or on-site services,... ...team.Theseniormedical writer will partner cross-... ...Operations,Biostatistics,Regulatory, and Program Management...Remote workSeniorRegulatoryLocal area
Synterex Inc
Princeton, NJ19 hours ago - ...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 treating...Remote workSeniorRegulatoryInterim roleWorldwide
Artivion
United States3 days ago - ...Senior Strategic Medical Writer AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health... ...Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support...Remote workSeniorRegulatoryTemporary work
Avery Healthcare Group Ltd.
United States1 day ago - ...Medical Writing Specialist For the past 25 years, ProPharma... ...With deep domain expertise in regulatory sciences, clinical research solutions, quality... ...less experienced medical writers, as necessary. Adheres... ...Whilst ProPharma supports remote working, we also recognize...Remote workSeniorRegulatoryContract workWork at office
ProPharma Group
Chicago, IL19 hours ago $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- ...seeking a Sponsor Dedicated Protocol Medical Writer II/Sr for a remote-based role. You will lead the... ...review of protocols, amendments, and regulatory submissions, ensuring accuracy and regulatory... ...junior writers. You will work with clinical scientists, data management, and...Remote jobSeniorRegulatory
$105k - $125k
...Environmental Conditions Office Job Description Senior Regulatory Medical Writer (FSP ; Remote; US ) At Thermo Fisher Scientific, you will... ...development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing...Remote workSeniorRegulatoryTemporary workWork at officeLocal areaFlexible hoursThermo Fisher Scientific
Framingham, MA4 days ago- ...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 jobSeniorRegulatory
- Syneos Health is seeking a Senior Medical Writer Publications for sponsor-dedicated work, primarily remote-based, to drive high-quality medical writing deliverables... ...lead content development, coordinate with clinical, regulatory, and biostatistics teams, ensure compliance...Remote jobSeniorRegulatory
- 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 throughout the product... ...you will author CERs, PMCF, and other clinical evidence documents, synthesize data...Remote jobSeniorRegulatory
- AbbVie is seeking a Senior Strategic Medical Writer to lead and author clinical and regulatory documents for drug and device development, supporting company objectives. The role requires strong expertise in medical writing across therapeutic areas, regulatory guidelines...SeniorRegulatory
- Stryker is hiring a Senior Staff Medical Writer for its Endoscopy Division. This remote, nationwide role focuses on developing regulatory and scientific documents to support global registrations... .... You will translate complex clinical evidence into CERs, PMCF, and other...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... ...possess 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
- Merck & Co. seeks a Clinical/Regulatory Medical Writer to develop and review regulated content across protocols, CSR, and public-facing documents, ensuring regulatory compliance and health-literacy standards. The role supports the CRSC within GCTO and partners with cross...SeniorRegulatory
- 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
- ...Full time Fully Remote Must be authorized to work... ...dedicated to providing top-tier medical writing services to... ...Role We're seeking a Senior or Principal Medical Writer to join our... ...lead writer on complex regulatory and clinical documents, provide strategic...Remote workSeniorRegulatoryFull timeLive inWork at officeFlexible hours
Eldridge Writing
Remote14 days ago - Senior Medical Writer/Principal Medical Writer Remote, United Kingdom Position Summary: The Senior Medical Writer/Principal... ...of high-quality and on-time clinical study documents. Specific... ...Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP) and...Remote workSeniorRegulatoryLocal area
- ...of highly experienced clinical development professionals specializing in medical writing, submission... ...support. Synterex offers remote or on‑site services,... ...writing team. The senior medical writer will partner cross‑functionally... ..., Biostatistics, Regulatory, and Program...Remote workSeniorRegulatoryLocal area
$75k - $112.5k
...demonstrating the economic, clinical, and societal value of creative medical treatments to payers,... ...Summary: The Senior Medical Writer is responsible for developing... ...medical, legal, regulatory review meetings and participate... ...content #LI-REMOTE Precision is...Remote workSeniorRegulatoryFull timeLocal area$85k - $100k
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: $85...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 jobRegulatoryContract work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Medical Writer — Remote (Regulatory/Clinical). Be the first to apply!
Related searches
- senior operations technician Denver, CO
- senior cloud service delivery manager Denver, CO
- senior it service manager Denver, CO
- senior project engineer Denver, CO
- senior chief engineer Denver, CO
- sr operations manager Denver, CO
- senior account director Denver, CO
- senior director clinical development Denver, CO
- sr accountant Denver, CO
- senior manager business development Denver, CO