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Healthcare
› Medical Writing
Medical Writing
1,297 open positions
Associate Medical Writer (Mandarin & English Language)
Iniziomedical
Nucleus Central - APAC
28d
Develop and deliver innovative medical communications projects including technical manuscripts, congress abstracts, posters, meeting reports, and educational materials.
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Medical Copywriter - Advertising
Realchemistry
London
28d
Medical copywriter creating commercially minded documents for healthcare professionals and patients, adhering to ABPI code of conduct.
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Regional Director, Medical Affairs - HIV
Msd
Singapore
28d
Lead execution of scientific and medical affairs plans for the HIV therapeutic area across an assigned region, driving alignment between global goals and local country needs.
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Senior Manager, Global Labeling Strategy
Bms
Warsaw-WeWork-PL
230k
28d
Drives global labeling strategy and manages the review/approval process for regulatory documents (CCDS, USPI, SmPC) to ensure compliance and timely submissions for low to medium complex projects.
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Regulatory Affairs Liaison (Associate Director)
Msd
SGP - Singapore - Singapore (Boulevard Towers)
28d
Associate Director leading regional regulatory strategy for product development, registration, and lifecycle management across the Asia Pacific region.
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Associate Director of Training- Patient Support Services
Sanofi
Cambridge, MA, US
28d
Design and execute comprehensive training strategies for Patient Support Services stakeholders, including case management, patient education, and field reimbursement teams.
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Senior Manager Global Regulatory Affairs CMC
Csl
EMEA, CH, Kanton Bern, Bern, CSL Behring
28d
Lead global regulatory CMC strategy for biological and non-biological product portfolios, managing submissions and compliance with regulatory agencies.
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Manager Med Info Ops (Hybrid & Night Shift)
Thermofisher
Taguig City, Philippines
28d
Lead medical information operations team to oversee development and dissemination of accurate medical and drug information, ensuring regulatory compliance and supporting healthcare professionals.
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Expert Scientific Writer HEVA
Sanofi
Hyderabad, IN
28d
Create HEVA communication deliverables (manuscripts, posters, abstracts, slide decks) and manage core HEVA communication processes to support healthcare decision makers with evidence on product value.
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Data Generation & Publication Manager
Ferring
Tokyo, Japan
28d
Lead the development and execution of evidence-generation plans (Phase IIIb/IV, HEOR, RWE) and integrated publication strategies to address scientific, clinical, and market access evidence gaps for pharmaceutical products.
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Indegene: Medical Information Manager (Canada)
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Trilogy Writing and Consulting
Toronto, ON, CA
CA$140k
28d
Deliver high-quality, balanced, and timely written or verbal medical and scientific information to healthcare professionals and consumers regarding pharmaceutical products.
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Associate Director, Global Media Relations
Bms
Princeton - NJ - US
$157k–$190k
28d
Shape and elevate Bristol Myers Squibb's global voice across business, trade, and consumer/lifestyle press to reach diverse audiences.
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Senior Manager Regulatory Affairs
Regeneron
Toronto, CA
28d
Develop globally aligned regulatory strategies for Canadian projects and manage Health Canada submissions.
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Associate Director, Global Media Relations
Bristolmyerssquibb
Princeton - NJ - US
$157k
28d
Shape and elevate Bristol Myers Squibb's global voice across business, trade, and consumer/lifestyle press to reach diverse audiences.
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Senior Manager, Global Labeling Strategy
Bristolmyerssquibb
Warsaw-WeWork-PL
230k
28d
Drives global labeling strategy and manages the review/approval process for regulatory labeling documents (CCDS, USPI, SmPC) to ensure compliance and timely submissions for low to medium complex projects.
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Vice President, Global Medical Lead - MASH
Madrigalpharma
PA - Conshohocken - Office, US
28d
Lead the integrated global medical strategy and plan for Madrigal's MASH portfolio, including Rezdiffra (resmetirom), aligning evidence generation, scientific engagement, and lifecycle planning to maximize patient impact and portfolio value.
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Lead Associate, Business Development
Dr-Reddy-S-Laboratories-Limited
Princeton, NJ, us
29d
Lead Associate managing licensing transactions (in-licensing/out-licensing) for Value Added Medicines, Biosimilars, and OTC/Self-Care portfolios to support North America growth.
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Senior Medical Writer - Medical Communications
Klick
Toronto, Ontario, ca
CA$110k–CA$135k
29d
Develop scientifically accurate, strategically aligned medical communications (manuscripts, abstracts, slide decks, advisory board reports) for life sciences clients across traditional and digital channels.
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Senior Medical Writer - Medical Communications
Klick
Philadelphia, Pennsylvania, us
29d
Develop scientifically accurate, strategically aligned medical communications including manuscripts, abstracts, posters, and digital content for life sciences clients.
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Chargé(e) de communication F/H
ECRIN EUROPEAN CLINICAL RESEARCH INFRASTRUCTURE NETWORK
Paris, Ile-de-France
29d
Execute clinical research communication strategy, manage internal/external communications, and organize international events.
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Expert Affaires Réglementaires F/H
AMARYLYS
Puteaux, Nanterre
29d
Specialized expert in pharmaceutical advertising control and marketing authorization (AMM) registration.
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Medical AQP Reviewer
AbbVie
Maidenhead, ENGLAND, gb
29d
Review and approve promotional and non-promotional meeting arrangements and materials for the UK Affiliate in compliance with the ABPI Code of Practice and other regulatory standards.
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Regulatory Affairs Officer-Registration
Adragos Pharma
Athens, Attiki, Greece
29d
Prepare EU/UK registration dossiers (Module 1) and manage lifecycle submissions for generic pharmaceutical products.
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RA Strategic Medical Writer
AbbVie
Minato City, Tokyo, jp
29d
Lead Japan-specific regulatory and clinical document preparation for pharmaceutical submissions, acting as a local coordinator between the Japan project team and global stakeholders.
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Manager, Expert Scientific Writer
Bms
Otemachi-JP
29d
Lead the authoring of clinical and regulatory documents for Phase 2/3 studies and submissions to the PMDA in Japan.
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Associate Regulatory Director
Bristolmyerssquibb
Beijing - CN
29d
Develop and implement regulatory strategies to achieve submission and approval for new products in a specific therapeutic area while ensuring compliance with government policies and company SOPs.
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Sr Medical Affairs Manager (Hybrid - Ontario, CA)
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Insulet Corporation
Oakville, ON, CA
CA$170k–CA$219k
29d
Develop and execute Medical Affairs strategy for Canada, leading evidence generation, medical education, and KOL engagement to support Omnipod product adoption.
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Medical - Scientific Strategy and Partnership Manager - Guangzhou
Sanofi
Guangzhou, CN
29d
Execute scientific strategic partnership plans with Centers of Excellence hospitals and academic institutions to align with overall scientific strategy.
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TA Head, Neurology
Biibhr
Shanghai, China
29d
Lead Neurology Medical teams to execute national medical strategies for Spinal Muscular Atrophy (SMA) and Amyotrophic Lateral Sclerosis (ALS), manage Patient Support Programs, and oversee people management.
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International Regulatory Affairs Manager
AstraZeneca
Petaling Jaya, Selangor, Malaysia
29d
Lead end-to-end planning, coordination, and execution of International Marketing Authorisation Applications (MAAs) and Clinical Line Extensions (CLEs) for drug development.
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Manager, Expert Scientific Writer
Bristolmyerssquibb
Otemachi-JP
29d
Lead the authoring of clinical and regulatory documents for Phase 2/3 studies and regulatory submissions to the PMDA in Japan.
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Associate Director, Medical Training & Compliance Lead
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Takeda Pharmaceuticals
KA, IN
29d
Design role-based onboarding and learning journeys, establish governance and training frameworks for Medical capabilities, and maintain an inspection-ready environment through effective SOP governance.
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Assoc Director, Regulatory Affairs
Gilead
Japan - Tokyo
29d
Develop and drive Japan labeling strategy across the product lifecycle, serve as the person in charge of CTD M1.8 and Japan Package Insert, and act as the Japan regulatory authority on labeling matters.
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Senior Director, Investor Relations
Bristolmyerssquibb
Princeton - NJ - US
$261k–$316k
29d
Serve as the primary interface between Bristol Myers Squibb and the investment community, driving global investor relations strategy, communicating key messages, and analyzing market data.
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Medical Editor
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Accenture
Remote
$64k
29d
Edits pharmaceutical and medical device creative pieces for content accuracy, AMA style, FDA regulations, and brand consistency.
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Senior Medical Director, EMEA
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Vantive
Remote
29d
Lead regional medical strategy for Acute and Vital Organ Therapies across EMEA while providing hands-on medical leadership for a key cluster.
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Manager, Regulatory Affairs
AstraZeneca
Mississauga, Ontario, Canada
$107k–$141k
29d
Lead regulatory strategies and submissions for assigned drug and biologic product portfolios to Health Canada.
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Therapeutic Area Medical Affairs Lead
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Organon Pharmaceuticals
London, ENG, GB
29d
Leading and developing a high-performing Medical Affairs team (Medical Advisors and Medical Science Liaisons) to execute medical strategy, product positioning, lifecycle management, and scientific exchange within a defined therapeutic area.
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Associate Director, Thought Leadership & Issues Communications
Bms
Princeton - NJ - US
$157k–$190k
29d
Execute global enterprise thought leadership strategy and support crisis/issues communications readiness for a life sciences company.
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International Regulatory Affairs Manager
AstraZeneca
Malaysia - Petaling Jaya
29d
Lead end-to-end planning, coordination, and execution of International Marketing Authorisation Applications (MAAs) and Clinical Line Extensions (CLEs) for small and large molecules.
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Associate Director, Thought Leadership & Issues Communications
Bristolmyerssquibb
Princeton - NJ - US
$157k
29d
Execute global enterprise thought leadership strategy and support crisis/issues communications readiness for a life sciences company.
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US Medical Director, Transplant CLAD
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Sanofi
Cambridge, MA
29d
Develop and execute US medical strategy for transplant products (specifically belumosudil/Rezurock) and support development in new therapeutic areas focusing on lung transplantation.
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Associate Director, U.S. Ethics & Compliance Advisor, Medical Affairs
Gilead
United States - California - Foster City
$182k–$236k
29d
Provide expertise in healthcare compliance ensuring Medical Affairs activities align with ethical standards and partner with Legal, Commercial, and Clinical Development to integrate compliance programs.
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(Sr.) District Manager
AbbVie
Qingdao, Shandong, cn
1mo
Manage regional business operations, resource allocation, and team development for the immunology therapeutic area.
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Medical Promo Review Contractor
OnQ Recruitment
Sydney, New South Wales
1mo
Review promotional and marketing materials for scientific accuracy, balance, and compliance before they progress through the medical approval pathway.
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Omnichannel Coordinator (Medical Affairs)
OnQ Recruitment
Sydney, New South Wales
1mo
Coordinate omnichannel engagement initiatives to deliver compliant scientific information to healthcare professionals via digital channels.
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Senior Global Regulatory Scientist
Ire
Remote
1mo
Provide high-level regulatory and scientific expertise to support global development strategies and submissions for new medicines and treatments.
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National MSL Director, Gastroenterology
AbbVie
Mettawa, IL, us
1mo
Establish strategy and provide oversight for the US Field Medical Team in Gastroenterology to achieve medical and business objectives.
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Senior Medical Director, Treatment - Global Medical Affairs, ViiV
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Gsk
London, ENG, GB
1mo
Provide senior global medical leadership for the long-acting HIV portfolio, establishing strategic direction and leading the evidence, communication, and launch-readiness agenda for an emerging treatment programme.
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Senior Regulatory Affairs Manager, Chemistry Manufacturing and Controls
Gehc
Remote, US
$106k
1mo
Provide CMC regulatory input and strategies to support development projects and marketed products in Pharmaceutical Diagnostics, developing and maintaining Quality sections of product dossiers (Module 2.3 and Module 3).
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