Senior Nonclinical Writer — Remote Leader
MMS Holdings Inc
- Remote job
MMS Holdings Inc. is seeking a Regulatory Nonclinical Writer for a full-time remote role. The candidate will develop and manage highly technical nonclinical documents to support regulatory submissions, including Module 2.4/2.6, IBs, and study reports, collaborating with cross-functional teams in a fast-paced environment. Ideal candidates have 5+ years of pharma regulatory nonclinical writing experience, strong writing/analytical skills, and knowledge of GLP and ICH guidelines, with proficiency #J-18808-Ljbffr MMS Holdings Inc
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$90k - $120k
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$55 - $75 per hour
...genetic diseases. This is a Contract role- Remote can live anywhere in the US- $55 to $75hour The Senior Medical Writer applies advanced documentation preparation... ...understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody...Remote workSeniorFull timeContract workFor contractorsWorldwideShift work- A leading CRO in Charleston, SC is seeking a Nonclinical Writer to develop and manage nonclinical documents. The ideal candidate will have 2+... ...strong analytical and communication skills. This full-time, remote role offers the opportunity to work in a collaborative and innovative...Remote jobFull time
$70k - $85k
A clinical research organization is seeking an entry-level regulatory writer to join their innovative team in Seattle. This full-time, remote position involves developing and managing nonclinical documents while collaborating with cross-functional teams. Candidates should...Remote jobFull time- A leading clinical research organization is seeking a technical writer to develop and manage nonclinical documents. This full-time remote position requires a BS in pharmacology or related fields, with a minimum of 2 years in regulatory writing. Candidates should possess...Remote jobFull time
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- Merck seeks an experienced Medical Writer to join the Nonclinical Pharmacology Documentation group. You will generate preclinical reports and submission modules, partner with research and regulatory functions, and manage multiple programs with competing timelines to meet...Senior
$132k - $151k
...Description Key Purpose: The Principal Medical Writer independently plans and prepares a range... .... Flexible, inclusive culture — 70% remote workforce, 66% women‑led teams. Learn... ...experience or equivalent experience with nonclinical sections of the CTD such as: 2.4...Remote workLocal areaWorldwideFlexible hours- Merck & Co., Inc. in California seeks an experienced Medical Writer to join our Nonclinical Pharmacology Documentation group, managing multiple preclinical programs and regulatory modules. You will collaborate with research and regulatory teams to produce high-quality...Senior
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