Senior Principal Medical Writer | Regulatory Dossier Lead
BeiGene, Ltd.
BeiGene, Ltd. is seeking a Medical Writer to develop high-quality clinical and regulatory documentation to support product lifecycle management. The role involves managing writing tasks, ensuring compliance with regulatory guidelines, and mentoring other writers. Candidates should have an advanced degree and extensive experience in regulatory document writing. Strong project management and communication skills are essential. A comprehensive benefits package is offered, including health insurance and stock options. #J-18808-Ljbffr BeiGene, Ltd.
$137.1k - $182.1k
...fit-for-purpose clinical and regulatory documents to facilitate speed... ...the working scope of global medical writing. This position is also... ...collaboration). Proactively leads direction and strategy setting... ...documents within the larger dossier and voices impacts on upstream...PrincipalSeniorRegulatoryFull timeFor contractorsLocal area- Veristat LLC is seeking a full-time Principal Medical Writer to independently plan and prepare regulatory documents and medical communications. This remote role involves supporting all phases of product development while collaborating with cross-functional teams. The ideal...PrincipalRegulatoryRemote jobFull time
$119.3k - $159.3k
BeiGene, Ltd. is seeking a Regulatory Writer to join its dynamic team in the United States. This role involves developing high-quality clinical and regulatory documents to ensure timely submissions of products. You will also mentor junior writers, ensuring compliance with...SeniorRegulatory$80.6k - $145k
A leading biopharmaceutical solutions organization seeks a Senior Medical Writer specializing in regulatory documents. This role involves leading the medical writing process, ensuring compliance with regulatory standards, and mentoring junior writers. Candidates should...SeniorRegulatory$80.6k - $145k
A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer specialized in regulatory documents. In this role, you'll lead the preparation of clinical documents and manage writing activities while ensuring compliance with regulatory guidelines....SeniorRegulatory- A leading biopharmaceutical solutions organization in Georgia is seeking a Senior Medical Writer specializing in regulatory documents. The selected candidate will lead medical writing deliverables for clinical studies, ensuring compliance with regulatory standards and high...SeniorRegulatory
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A leading biopharmaceutical solutions organization in New Jersey is seeking a Senior Medical Writer to manage and complete regulatory documents. Responsibilities include writing clinical study protocols, ensuring adherence to regulatory standards, and mentoring junior writers...SeniorRegulatoryFlexible hours- Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced medical writer in Georgia. The role involves leading medical writing projects, ensuring compliance with regulatory standards, and mentoring junior writers. You will create clinical documents and engage...SeniorRegulatoryFlexible hours
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A clinical-stage biopharmaceutical firm is seeking a Medical Writer to support clinical development programs. The candidate will be responsible for producing high-quality regulatory documents and collaborating with cross-functional teams to ensure compliance. Requirements...SeniorRegulatoryRemote job$80.6k - $145k
...Health/ inVentiv Health Commercial LLC in Kentucky is seeking a Medical Writer to lead clear and accurate medical writing projects. The successful... ...include completing clinical documents, adhering to regulatory standards, and mentoring junior writers. The position offers...SeniorRegulatoryContract workFlexible hours- A leading biotechnology company in Idaho is seeking a Senior Principal Scientist as a Project Toxicologist to lead nonclinical safety strategies. The role involves... ...a doctoral degree and extensive experience in regulatory document authoring and toxicology, adapting strategies...PrincipalSeniorRegulatory
$187.27k - $318.26k
...analytic product portfolio. In this senior individual contributor role,... ...financial data domains and regulatory considerations (e.g. privacy... ...and regulatory expertise ~ Lead across cross-functional teams... ...at a senior level (Director, Principal, or Head of Product...PrincipalSeniorRegulatoryFull time- argenx SE is seeking a Senior Medical Writer to author and manage contributions for regulatory submissions, ensuring compliance with medical writing standards. The successful candidate will have a strong background in pharma or biotech, with at least 3 years of clinical...SeniorRegulatory
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A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer specializing in regulatory documents. This role involves managing medical writing activities, ensuring compliance with regulatory standards, and mentoring junior writers. The ideal candidate...SeniorRegulatory- ...Infosys Consulting is seeking a Principal to lead engagements in Financial Crimes, focusing on AML Transaction Monitoring and KYC/CDD. The... ...delivery teams, developing strategies, and advising clients on regulatory compliance. The ideal candidate has at least 10 years in...PrincipalSeniorRegulatory
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Holthouse Carlin & Van Trigt LLP, based in New York, is searching for a Tax Manager to oversee the review of federal and multi-state income tax returns. The successful candidate will have over 10 years of technical tax experience, including leadership in managing teams...PrincipalSenior- A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer for a remote position. This role involves managing medical writing deliverables, coordinating... ...departments, and ensuring compliance with regulatory standards. Candidates should have...SeniorRegulatoryRemote jobFlexible hours
$62k - $108.6k
Principal/Sr Medical Editor - Regulatory Documents - Copy Editing + QC - NA/Canada Remote Based Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate... ...and updates the lead medical writer, project manager, and/or direct...PrincipalSeniorRegulatoryRemote jobContract workFlexible hours$80.6k - $145k
...Health/ inVentiv Health Commercial LLC is seeking a Medical Writer in Oklahoma. This role involves leading medical writing activities, ensuring the clarity... ...accuracy of various clinical documents, and adhering to regulatory standards. Candidates should have 3-5 years of...SeniorRegulatoryFlexible hours- A leading data-focused CRO is seeking a Remote Senior Medical Writer to contribute to clinical development documents and mentor team members. Candidates should have strong writing skills, at least three years of experience in the pharmaceutical industry, and an educational...SeniorRegulatoryRemote jobFull time
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- Principal Medical Writer, Brand & Promotion Remote, United Kingdom Precision AQ... ...materials. Working with a Senior Scientific Director (SrScD)... ...Medical Writer (PMW) leads content development across... ...meetings, and medical‑legal‑regulatory (MLR) review sessions. Act...PrincipalRegulatoryRemote work
$119.3k - $159.3k
...General Description As a key member of the regulatory writing team, you will develop high‑... ...pipeline. You will also mentor junior medical writers (full‑time employees and/or contractors... ...including complex or urgent projects. Lead document development strategy, collaborate...PrincipalRegulatoryFull timeFor contractors$80.6k - $145k
Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Medical Writer to ensure clear and accurate medical writing deliverables. The role demands 3-5 years of relevant experience, strong knowledge of FDA/ICH regulations, and a track record in the biopharmaceuticals...Senior- Clark Davis Associates, Inc is seeking a Senior Medical Writer to join their top pharmaceutical team in the US. This remote role involves reviewing... ..., mentoring junior writers, and ensuring adherence to regulatory standards. The ideal candidate should have a Bachelor’s...SeniorRegulatoryRemote job
- 6AM City, LLC is seeking an experienced Medical Writer to join their team. The role involves writing and editing clinical development documents... ...other writers. Candidates should have a strong background in regulatory writing within the pharmaceutical industry, with at least 3-5...Regulatory
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