Senior Nonclinical Medical Writer: Lead Preclinical Submissions
MSD Malaysia
Merck & Co., Inc. seeks an experienced Medical Writer to join the Nonclinical Pharmacology Documentation group. You will generate preclinical reports and regulatory submission modules, partnering with research and regulatory teams to ensure high-quality scientific and regulatory documents across multiple programs. The role requires managing multiple programs, prioritizing timelines, and driving completion in alignment with regulatory milestones. #J-18808-Ljbffr MSD Malaysia
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$120 - $175 per hour
...penfieldsearch.comNo 3rd party candidatesLocation: Bay Area-based roleWork Model: 5 days onsite per weekWe are seeking a Senior Regulatory Submission Lead to support a critical BLA submission across Module 2 and Module 5. This 1 year contract role will provide hands-on...SeniorHourly payContract work- Position Title: Senior Medical Content Writer Work Location: South San Francisco, CA Assignment Duration: 3 Months Work Schedule: Monday through... ...and claim substantiation packages ready for MLR submission. Write medical content across formats: HCP materials, patient...SeniorWork at officeMonday to Friday
$182.1k - $338.3k
...world where we all have more time with the people we love. Medical Operations Education & Communication (MOEC), a function in... ...accessible and affordable for all.The Principal Content & Evidence Submission Strategy Lead is focused on developing the medical communications...Full timeLocal area$171k - $223k
...level Toxicologist with over 10 years of industry experience to lead nonclinical safety strategies across discovery and development stages.... ...mentoring junior scientists, providing input on regulatory submissions, and developing innovative toxicology processes. We offer a...Senior- ...hours/week) to manage a variety of writing and editing projects, including Clinical Study Protocols, amendments, CSRs, regulatory submissions and DSUR responses. The role requires extensive experience in clinical/regulatory writing within biotech, strong communication...Remote jobContract workPart timeFor contractors
$131.4k - $206.8k
Job Description We are seeking an experienced Medical Writer to join our Nonclinical Pharmacology Documentation group responsible for the generation of preclinical reports and submission modules to support development programs ranging from FIH to global marketing applications...SeniorFor contractorsWork at officeLocal area- ...Therapeutics in South San Francisco seeks an Associate Director, CMC Program Management to lead CMC strategies, deliverables, and timelines across development stages, including NDA/MAA submissions. You will manage CRO/CMO vendors and guide cross-functional teams to integrate CMC...Senior
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$244k - $305k
.... The Opportunity: The Senior Director, Molecule Global Regulatory Lead will develop and execute... ...teams. Regulatory Submission Leadership Provide strategic... ...Regulatory Operations, Medical Writing, Clinical... ...Clinical Operations, Safety, Nonclinical, CMC, Biometrics,...SeniorFull timeLocal area$186k - $233k
...experienced Statistical Programmer with over 14 years in oncology trials. The role entails leading studies, collaborating with teams, and overseeing programming support for regulatory submissions in a dynamic environment. This opportunity offers competitive pay, from $186,000...Senior- ...This role involves developing and implementing project plans, ensuring regulatory strategy execution, and overseeing regulatory submissions both pre- and post-approval. Candidates should have a minimum of 8 years in regulatory development within the pharmaceutical industry...Work at office
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$154.89k - $176.98k
...therapies for people with unmet medical needs. Since 2004,... ...Statement The mission of the Preclinical Development team is to attract... ...therapeutic candidates toward IND submission and clearance Experience... ...Supervision Received The Senior Science Officer I reports directly...SeniorCasual workWork at officeRemote work- Mill is seeking an experienced Sustaining Program Manager to own the day-to-day program management of Mill's Consumer hardware line as it scales from launch into steady-state production. You will drive sustaining engineering, supply chain activities end to end, engineering...Senior
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