Temporary Principal Regulatory Writer - Global Submissions
$180 per hourVir-Biotechnology
Vir Biotechnology is seeking a Principal Regulatory Writer to handle regulatory submissions, collaborating with senior management to ensure compliance and quality. The ideal candidate will have 15–20 years of experience in regulatory writing and a Bachelor's degree, with expertise in clinical trial documents and eCTD structures. Compensation ranges from $180 to $200 per hour based on qualifications. #J-18808-Ljbffr Vir-Biotechnology
$95k - $210.9k
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredSyneos Health is a leading fully-integrated... ...documents for submissions to regulatory authorities globally.Provides strategic direction to cross-functional...PrincipalRegulatoryContract workFlexible hours- Vir Biotechnology is seeking a Senior Regulatory Writer to support regulatory submission writing. This role requires collaboration with senior management and other leads to ensure consistent messaging and compliance. The successful candidate will have extensive experience...Regulatory
$95k - $105k
...+ Assign tasks to internal writers and freelancers, managing workflow... ..., ensuring compliance with submission requirements. + Revise... ..., adhering to medical/legal/regulatory (MLR) review process requirements... ....**Position Overview:** The Principal Medical Writer is...Temporary workPrincipalRegulatoryFreelance$137.1k - $182.1k
...high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and lifecycle management of products... ...documents within the working scope of global medical writing. This position is also responsible...PrincipalRegulatoryFull timeFor contractorsLocal area- Otsuka Pharmaceutical Co., Ltd is seeking a skilled regulatory affairs professional to provide critical support in developing global regulatory strategies and managing submissions for investigational and marketed prescription drugs. Candidates should have a relevant degree...Regulatory
$82k - $164k
Join to apply for the Principal Specialist, Global Trade (Remote) role at Raytheon Join to apply for the Principal Specialist, Global Trade (Remote... ...applicable trade compliance records in accordance with regulatory requirements. Development and implementation of...Temporary workPrincipalRegulatoryRemote jobFull timeWork experience placementWork from homeFlexible hours$172.5k - $222.5k
Principal Creative, Copy Circle is one of the world's leading internet... ...foundation of a more open, global economy through digital assets... ...thinker and a hands-on writer, developing creative content... ...write within compliance and regulatory frameworks. A flexible, self-...PrincipalRegulatoryFlexible hours- 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...Regulatory
$176.4k - $228.25k
...Neura Market is seeking a Manager/Director of CMC Regulatory Affairs to lead the development and implementation of regulatory strategies... ...to facilitating clinical research and ensuring compliance with global regulatory standards. The ideal candidate will have 8+ years...RegulatoryRemote work$85k - $100k
...relations activities. The RFP Writer will primarily support... ...and as part of a global team. Reporting Relationship Reports to: Principal, Global Client... ...strategies ensuring a timely submission. Provide back‑up... ...management advisory, financial regulatory environment, or...Temporary workRegulatoryWork experience placementWork at officeFlexible hours- Principal Risk Manager - Global Payments Network Risk Are you ready to lead from the front line of a top 10 bank? Do you thrive in a high-visibility... ...flawless documentation that aligns with complex regulatory and internal expectations. Framework Alignment: Map and...PrincipalRegulatoryFull timePart timeLocal area
$146.41k - $192.16k
...Legend Biotech is a global biotechnology company dedicated to treating, and one day... ...Position Legend Biotech is seeking a Principal Scientist, Lentivirus Upstream Process... ...development reports, SOPs, and CMC sections for regulatory submissions (IND). Work closely with Downstream...Temporary workPrincipalRegulatoryPermanent employmentFull timeFor contractorsLocal areaWorldwideFlexible hours$109.9k - $125.4k
...Principal Associate, Risk and Compliance, Global Workplace Services At Capital One, we dare to dream, disrupt and deliver a better way. Our goal is simple... ...an understanding of enterprise risk, governance, regulatory, and change management frameworks Contribute to...PrincipalRegulatoryFull timePart timeWork at officeLocal area- ...leading healthcare intelligence firm is seeking a Principal Medical Writer to lead the development of regulatory and clinical documents. The ideal candidate will... ...writing experience, particularly in regulatory submissions. This role offers a competitive salary and a...RegulatoryRemote jobFlexible hours
$24 - $32.5 per hour
...of the Year, and has been recognized by Global Trade Americas as a leading 3PL to watch... ...hour Responsibilities The Custom Entry Writer is responsible for preparing, collating,... ...of all issues. Research and assist with regulatory questions. Review and monitor customs clearances...Temporary workRegulatoryHourly payWork at officeWorldwide- 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...PrincipalRegulatory
- 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
$140k - $160k
Iovance Biotherapeutics is seeking a Manager, Regulatory Affairs CMC to oversee regulatory submissions and collaborate with cross-functional teams. The ideal candidate will have at least 8 years of experience in regulatory affairs and a BA/BS degree in a related field....Regulatory$210k - $260k
Role and Responsibilities Lead Global Platform Strategy: Define and execute the product roadmap for our expansion into new global information... ...compliant XML filings across multiple jurisdictions. Translate Regulatory Nuance into Product Reality: Partner closely with Tax SMEs to...PrincipalRegulatory$120k - $160k
...career opportunity for anS4 Hana Principal Config Analyst. This position... ...to govern end-to-end global trade compliance processes, including... ...business, financial, and regulatory requirements, recommending operational... ...contract. Depending on your temporary assignment, benefits may...Temporary workPrincipalRegulatoryContract workFor contractorsLocal areaRemote work$205k - $341.6k
Regeneron Pharmaceuticals, Inc. is seeking a Director for Regulatory Affairs Strategy to provide leadership on global regulatory activities for the Genetic Medicine portfolio. This role involves regulatory strategy, filings, and mentorship of regulatory staff. The ideal...Regulatory$163.4k - $241.82k
...The Challenge As Director, Global Affairs (Americas), you will... ...implementing legislative and regulatory advocacy strategies on a broad... ...discussions, meetings, and submissions. Represent Take-Two at... ...other benefits, provided that temporary or intern roles will not be...Temporary workRegulatoryCasual workInternshipFlexible hours- Praxis Precision Medicines, Inc. is searching for a Senior Regulatory Submissions Manager to oversee regulatory submissions to U.S. and international agencies. The role requires at least 7 years of experience in the pharmaceutical or biotech industry and strong management...RegulatoryRemote job
$85k - $160k
...Wealth Marketing, PWM Content Writer, Associate - New York New... ...editorial, subject matter, and regulatory reviews to ensure content meets... ...in 1869, we are a leading global investment banking, securities... ...generally available to active, non-temporary, full-time and part-time US...Temporary workRegulatoryFull timePart time$32.11 - $57.91 per hour
...provider-focused copy Familiarity with MLR (Medical/Legal/Regulatory) review and Veeva PromoMats Conceptual and tactical writing... ...Company reserves the right to modify this pay range at any time. Temporary roles may be eligible to participate in our freelancer/...Temporary workRegulatoryHourly payFull timePart timeFreelanceRemote workWorldwideFlexible hours- Principal Medical Writer, Brand & Promotion Remote, United Kingdom Precision AQ is growing! We are seeking an exceptional Principal Medical... ...and external experts in calls, meetings, and medical‑legal‑regulatory (MLR) review sessions. Act as the scientific lead for assigned...PrincipalRegulatoryRemote work
- ...less alone. How You Will Make an Impact Frida is seeking a Global Regulatory Manager (Contractor) to join our Quality and Regulatory team... ...products and the preparation/review of international regulatory submission(s) (EU MDR Tech File, Health Canada submission, Saudi FDA,...Temporary workRegulatoryContract workFor contractorsWork at officeLocal areaImmediate startRemote work
$150k - $300k
...Global Banking & Markets, Prime Business Negotiations, Vice President... ...for negotiating trading and regulatory documentation across a... ...premier global business. PRINCIPAL RESPONSIBILITIES Strategic... ...generally available to active, non-temporary, full-time and part-time U.S....Temporary workRegulatoryFull timePart timeWorldwide- Our client, a leading global biopharmaceutical company, is seeking a Principal PK/PD Scientist to provide scientific leadership... ...support clinical development, regulatory interactions, and portfolio... .... Contribute to regulatory submissions, briefing packages, and responses...PrincipalRegulatory
- Our client, a leading global biopharmaceutical company, is seeking a Principal PK/PD Scientist to provide scientific leadership... ...design, dose selection, and regulatory strategy. Collaborate with... ...-making. Support regulatory submissions and interactions with global health...PrincipalRegulatory
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