Senior Medical Writer Remote (Regulatory/Clinical)
MMS Holdings Inc.
- Remote job
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 for maintaining project timelines and mentoring team members while ensuring compliance with rigorous standards. Exceptional writing skills, proficiency with MS tools, and a background in scientific disciplines are essential for this role. #J-18808-Ljbffr MMS Holdings
- ...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 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
- MMS, a data-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 leadership of project teams, strong communication with clients...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
- 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
- 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
- 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
$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 jobSeniorRegulatory- ...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
- ...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
- ...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
- .... 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
$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- ...Inc. is seeking a Sponsor Dedicated Protocol Medical Writer II/Sr for US/Canada remote work. The role partners with Clinical Scientists to lead protocol writing,... ...coordinate with data management, biostatistics, regulatory, and medical affairs teams. #J-18808-Ljbffr...Remote jobSeniorRegulatory
- ...Senior Medical Writer At ICON Strategic Solutions, you will work in a sponsor-dedicated model,... ...execution of medical writing strategies for clinical research projects, contributing to the... ...Independently produces clinical and regulatory documents in collaboration with...Remote workSeniorRegulatoryWorldwide
- Join MMS, an award-winning data-focused clinical research organization, as a Medical Writer. This full-time, UK-remote role focuses on producing regulatory medical writing deliverables with rigorous scientific standards. You will write and edit protocols, investigator brochures...Remote jobSeniorRegulatoryFull time
- 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
$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$128k - $176k
...patients. For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory submissions. This individual will execute the overall...Remote workSeniorRegulatoryTemporary work- ...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
- ...solutions company is seeking a Sr Medical Writer to lead medical writing... ...and ensure compliance with regulatory standards. Responsibilities... ...managing writing activities for clinical studies, completing diverse... ...ICH guidelines. The role is remote-based and offers competitive...Remote jobSeniorRegulatoryFlexible hours
$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- ICON invites a Senior Medical Writer to lead the development of medical writing strategies for clinical research projects. You will craft CPP documents... ...materials to support regulatory submissions and trial... ...a fast-paced environment. #J-18808-Ljbffr Remote Worker LTD.Remote jobSeniorRegulatory
- ...research and discovery to post-market clinical development, our WWRD engine involves... ...genetic diseases. ROLE: The Senior Medical Writer applies advanced documentation... ...reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES...Remote workSeniorRegulatoryFull timeFor contractorsWorldwideShift work
$101.7k - $136.7k
...Senior Medical Writer BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals... ...is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international regulatory...Remote workSeniorRegulatoryHourly payContract workLocal areaShift work- ...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
- Synterex, Inc. is seeking a Senior Medical Writer to join their team remotely. This role involves leading the planning and preparation of clinical regulatory documents while collaborating with various departments. The ideal candidate has over 5 years of experience in medical...Remote jobSeniorRegulatory
$90k - $140k
...Senior Medical Writer Everest Clinical Research ("Everest") is a full-service contract research organization... ..., Canada on-site location, or remotely from a home-based office anywhere... ...and succinct documents supporting regulatory submissions for clinical trial authorizations...Remote workSeniorRegulatoryContract workTemporary workWork from homeWorldwide- TransPerfect is seeking a senior medical writer to lead the planning and preparation of high-quality regulatory documents across Clinical Development, Regulatory, and Program Management.... ...a bachelor's degree or higher. Fully remote in the US with on-site client meetings...Remote jobSeniorRegulatory
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