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
$70.1k - $145k
Syneos Health/inVentiv Health Commercial LLC is seeking a Senior Medical Writer in Georgia, United States. The role involves overseeing medical writing deliverables, ensuring regulatory standards are met, and collaborating with clients and departments. The ideal candidate...SeniorRegulatory- PRIME Therapeutics is seeking a Senior Principal Government Affairs Policy Advisor to manage State and Federal policy functions. This position requires establishing partnerships with executive leadership and providing strategic policy insights. The ideal candidate will...PrincipalSeniorRegulatoryRemote job
- 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...SeniorRegulatoryRemote job
- 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... ...and possess exceptional communication and regulatory knowledge. Competitive salary and benefits,...SeniorRegulatoryRemote jobFixed term contract
- 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
$95k - $210.9k
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredSyneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every...PrincipalSeniorRegulatoryContract workFlexible hours- Langland is hiring a Principal Medical Writer in the United States, responsible for leading and mentoring a medical writing team, setting editorial direction, and delivering high-quality scientific content. The ideal candidate will have over 5 years of experience within...Principal
- 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
- A biopharmaceutical solutions company is seeking a Sr Medical Writer to lead medical writing deliverables and ensure compliance with regulatory standards. Responsibilities include managing writing activities for clinical studies, completing diverse documents, and mentoring...SeniorRegulatoryRemote jobFlexible 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
- Syneos Health is seeking a Senior Medical Writer to play a pivotal role in creating and coordinating high-quality medical documents for clinical and regulatory projects. This is a critical function that involves collaborating closely with various teams to ensure that writing...SeniorRegulatory
- ...A biopharmaceutical company is seeking a Senior Manager, Global Regulatory Affairs Labeling to lead its global labeling initiatives. This role involves strategy development for labeling, ensuring compliance, and managing cross-functional stakeholder reviews. Candidates...SeniorRegulatoryRemote work
- 1001 Syneos Health, LLC is seeking a Medical Writer II/Senior Medical Writer to lead medical writing for clinical studies and regulatory projects. This role involves writing, editing, and ensuring content adherence to regulatory standards. Applicants should have 3-5 years...SeniorRegulatoryFlexible hours
$95k - $105k
...leaders. + Assign tasks to internal writers and freelancers, managing workflow and... ...during the project lifecycle, adhering to medical/legal/regulatory (MLR) review process requirements.* *... ...notice.**Position Overview:** The Principal Medical Writer is responsible for the...PrincipalRegulatoryTemporary workFreelance- 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
$95k - $105k
A leading healthcare communications firm is seeking a Principal Medical Writer to develop high-quality medical content targeted toward healthcare professionals. The ideal candidate should have an advanced degree in a healthcare-related field and at least 3 years of experience...Senior- A leading healthcare intelligence firm is seeking a Principal Medical Writer to lead the development of regulatory and clinical documents. The ideal candidate will have an advanced degree in life sciences and significant medical writing experience, particularly in regulatory...RegulatoryRemote jobFlexible hours
- Overview Senior Medical Writer (Remote) at MMS. Join to apply for the Senior Medical Writer (Remote... ...approach to complex trial data and regulatory submission challenges. With a global footprint... ...with clinical study protocols as lead author. Experience leading and...SeniorRegulatoryRemote jobFull time
- ...development professionals specializing in medical writing, submission publishing,... ...our medical writing team. The senior medical writer will partner cross‑functionally... ...Operations, Biostatistics, Regulatory, and Program Management to lead the planning and preparation of...SeniorRegulatoryLocal areaRemote work
$115k - $185k
...A medical device company is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and strategy for new product development. This role offers flexibility in levels and can be remote, aligned with US East Coast hours. Candidates should have a Bachelor...SeniorRegulatoryRemote work$128k - $176k
Senior Medical Writer Join us as we transform immunology and deliver medicines that help autoimmune... ...contribution to develop content for regulatory submissions that is well‑organized, consistent... ...writing activities. Supports the lead writer and project teams to ensure...SeniorRegulatoryTemporary work- ...Title: Senior/ Principal Statistical Programmer(R) Location: Remote Duration: Long Term Contract Salary: Open Experience : 6-10+ Years Notice... ...SAS , solid CDISC (SDTM/ADaM) experience, and exposure to regulatory deliverables (TLFs, ISS/ISE, submissions). Mandatory Skills...PrincipalSeniorRegulatoryLong term contractImmediate startRemote work
$140k - $190k
SLR Consulting is seeking a Principal Engineer in New Jersey. This senior leadership position involves driving business development and leading strategic environmental projects. The ideal... ...project finances, ensuring regulatory compliance, and mentoring junior staff...PrincipalSeniorRegulatoryRemote job$82.92k - $150k
...A leading cryptocurrency exchange is seeking a Senior Compliance Officer to develop and implement compliance programs related to BSA/AML and KYC regulations... ...flexibility in a dynamic environment focused on regulatory compliance and risk mitigation. #J-18808-Ljbffr...SeniorRegulatoryRemote work- Civil & Environmental Consultants, Inc. is seeking an Air Quality Senior Project Manager/Principal to lead air permitting and regulatory compliance programs in our Cincinnati, OH office. You will manage complex air quality projects and mentor junior staff while developing...PrincipalRegulatoryWork at office
- Financial Industry Regulatory Authority, Inc. is looking for a Senior Principal Analyst to conduct essential research and analysis in Market & Regulatory Services. This role focuses on assessing opportunities, risks, and costs for new products and services, ensuring alignment...PrincipalSeniorRegulatory
$220k - $250k
...The successful candidate will lead our engagement with clients,... ...support strategy with global senior colleagues and managing the delivery... ...litigation, arbitration, regulatory and governance, insolvency... ...flexible and remote working. Medical Benefits, Prescription Benefits...PrincipalRegulatoryWork at officeRemote workFlexible hours- Initial Therapeutics, Inc. is seeking a Senior Manager for their Regulatory Affairs Advertising and Promotion team in the United States. This role involves managing regulatory activities for advertising and promotion of marketed products, ensuring compliance with FDA regulations...SeniorRegulatory
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