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Healthcare
› Medical Writing
Medical Writing
1,296 open positions
Medical Education Manager Latam
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Bd
São Paulo, SP, BR
8d
Develop and execute local educational strategy for designated areas, aligning with business needs and overall strategy to ensure continuous communication and alignment with commercial partners.
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Senior Account Manager
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Cactus Communications Services Pte. Ltd.
MH, IN
8d
Manage accounts and standard projects independently for global biopharma clients, ensuring delivery on budget and schedule while strengthening client partnerships.
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Senior Medical Writer
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Cactus Communications Services Pte. Ltd.
Remote
8d
Develop, review, and proofread high-quality scientific, medical, and educational materials (slides, abstracts, posters, infographics, digital content) for pharmaceutical clients.
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Specialist Regulatory Affairs
Organon
SGP - Singapore - Singapore
8d
Manage regulatory submissions and lifecycle management for pharmaceutical products in Singapore and Brunei to ensure compliance with local legislations and company procedures.
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Medical Director
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Exeltis UK
London Area, United Kingdom
8d
Senior medical leader accountable for providing medical and scientific leadership across the product portfolio and therapeutic areas for the UK affiliate.
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Director, Medical Affairs EMEA
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Tandem Diabetes Care
8d
Lead Medical Affairs strategy, evidence generation, and medical engagement for Tandem's insulin pump systems across the EMEA region.
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Global Medical Lead - Dermatology (UK)
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Ucb
England, United Kingdom
8d
Provide strategic global medical and scientific leadership across Dermatology, focusing on hidradenitis suppurativa, translating science into value for patients and healthcare professionals.
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Mandarin Medical Information Specialist
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ProPharma
Remote
8d
Deliver accurate, evidence-based medical information and safety responses to healthcare professionals and patients for pharmaceutical clients in Mainland China.
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Medical Advisor-Haematology
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Dr. Reddy's Laboratories
Hyderabad, Telangana, India
8d
Provide the scientific foundation for the Therapeutic Area medical strategy, manage medical activities, and engage key thought leaders.
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Medical Writer
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Quanticate
Bengaluru, Karnataka, India
8d
Lead and contribute to medical writing projects, authoring and quality-checking regulatory and scientific documents for clinical development programmes.
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FSP Regulatory Affairs Manager - Regulatory Intelligence MC
Thermofisher
Remote, Belgium
8d
Provide strategic regulatory intelligence and guidance to support pharmaceutical product development from preclinical stages through registration, monitoring global regulatory developments and translating them into actionable insights.
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Director, Global Oncology Publications
AstraZeneca
Gaithersburg, Maryland, United States of America
$193k–$290k
8d
Lead the development and execution of the publication strategy and tactical plan for global clinical studies in humans from Phase Ib-IV, and non-clinical trial sources including health economics and outcomes research, epidemiology, real-world evidence, payer…
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Director, Promotional Regulatory Affairs
AstraZeneca
Wilmington, Delaware, United States of America
8d
Strategic leadership in FDA promotional regulations, providing expert guidance and risk assessments for promotional materials across assigned brands.
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Manager - Medical Affairs (LATAM)
ConvaTec
Sao Paulo, Brazil
8d
Lead Medical Affairs strategy for Convatec's wound care, ostomy, and continence products across Latin America by building KOL networks, generating clinical evidence, and driving clinical practice adoption.
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Executive Director, International Medical Affairs, Dermatology
Novartis
Basel (City), CH
185k–343k
8d
Lead international medical strategy, evidence generation, and scientific engagement for the Dermatology portfolio across global markets.
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Global Labelling Manager, Content
Novartis
London (The Westworks), GB
£57k–£105k
8d
Develop and maintain global product labelling documents for neuroscience medicines, translating clinical and safety data into compliant information for healthcare professionals and patients.
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Executive Director, International Medical Affairs, Rheumatology
Novartis
Basel (City), CH
185k–343k
8d
Lead international medical strategy and team for Rheumatology portfolio across pipeline, pre-launch, launch, and lifecycle management to support clinical adoption and patient access globally.
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Associate Director, US Medical Promotional Review Scientist, Neuroscience
Bristolmyerssquibb
Princeton - NJ - US
$156k–$188k
8d
Ensure medical accuracy and scientific validity of promotional and non-promotional materials for Neuroscience brands while maintaining compliance with US laws and regulations.
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Senior Manager, Project Manager, Franchise Strategy & Operations
Bms
Princeton - NJ - US
$123k–$149k
8d
Strategic and operational portfolio partner for the medical lead, responsible for planning, risk mitigation, and delivering portfolio priorities including medical meetings, budget management, and congress activities.
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Associate Director, Promotional Regulatory Affairs (BBU)
AstraZeneca
Gaithersburg, Maryland, United States of America
$150k–$225k
8d
Lead regulatory review and risk assessment of pharmaceutical promotional materials to ensure compliance with US FDA regulations and support business initiatives.
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US Scientific Communications Senior Director
AstraZeneca
Wilmington, Delaware, United States of America
$197k–$296k
8d
Sets the strategic agenda for the US medical communications function, building a high-performing team to define content development strategy and improve the quality and impact of scientific communications deliverables.
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Director Promotional Regulatory Affairs
AstraZeneca
Gaithersburg, Maryland, United States of America
8d
Set regulatory guardrails for US promotional materials across healthcare professionals, consumers, and payers to ensure compliance and accelerate brand execution.
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Journal Development Editor (m/f/o) with focus on Sustainability and Life Science Portfolio
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Georg Thieme Verlag
DE
8d
Develop and manage the chemical sciences journal portfolio, including new launches and acquisitions, while driving open access strategy and ensuring publishing quality.
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Executive Medical Director, Regional Medical Affairs, CEEM Region
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Vertex Pharmaceuticals
München, BY, DE
8d
Executive leadership of Regional Medical Affairs strategy, governance, and execution across the CEEM region to facilitate product launches and align with global objectives.
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CVRM Medical lead (Biopharma & RD)
AstraZeneca
South Korea - Seoul, KR
8d
Medical leader responsible for a team within a Therapy Area or significant product, ensuring business unit goals are achieved through strategic direction, standards setting, and scientific leadership.
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Regulatory FSP Director CMC Lead - EMEA
Thermofisher
Sofia, Bulgaria
8d
Senior technical and operational leadership for CMC regulatory services, supporting Functional Service Provider (FSP) teams and clients in clinical trial authorization, marketing authorization, and product lifecycle management.
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Global Regulatory Lead
Csl
Americas, US-PA, King of Prussia, CSL Behring
$242k–$270k
8d
Develop and lead innovative, science-driven global regulatory strategies for assigned products across the product lifecycle, serving as the primary Global Regulatory Affairs representative on Product Strategy Teams.
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Field Medical Excellence Advisor
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Ferrer
Barcelona, Catalonia, Spain
8d
Create and improve tools, resources, and data strategies to enhance the effectiveness of global field medical teams and ensure regulatory compliance.
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Publications Specialist
Pfizer
India - Chennai
8d
Managing global publication plans for multiple products across therapeutic areas, supporting Scientific Publication Committees (SPCs), and overseeing budgets and vendors.
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Medical Director, Dyslipidemia
AstraZeneca
US - Wilmington - DE
$193k–$290k
8d
Lead the development and execution of US Medical strategy for dyslipidemia and related assets, translating disease area priorities into actionable medical execution plans and transforming care initiatives.
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Assoc Director, Regulatory Affairs
Gilead
Japan - Tokyo
8d
Lead regulatory submissions and strategy for investigational and commercial products across assigned territories, ensuring compliance with ICH and regional requirements.
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Group Lead – Content Approval Excellence & Content Operations
Sanofi
Hyderabad, IN
8d
Design, govern, and continuously improve the operating framework for Scientific Communications content lifecycle, ensuring high-quality, efficient, and scalable delivery through process excellence, quality-at-source principles, and technology integration.
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Associate Director, US Marketing Ophthalmology, Patient Experience Measurement & Engagement
Msd
USA - Pennsylvania - North Wales (Upper Gwynedd)
8d
Define and execute patient experience measurement strategies and engagement programs for investigational ophthalmology therapies to improve treatment continuity and patient outcomes.
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Associate Director, Promotional Regulatory Affairs
AstraZeneca
US - Gaithersburg - MD
$150k–$225k
8d
Lead review and adjudication of promotional materials for pharmaceutical products in the US, providing regulatory guidance and risk assessment to ensure compliance with FDA regulations.
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China Regulatory CMC Lead
Biibhr
Shanghai, China
8d
Senior in-country Regulatory CMC leader setting China CMC regulatory direction, interpreting evolving regulations, and translating them into enterprise-level strategies across development, registration, and lifecycle management.
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【医学部】ONC Hematology Medical Lead
Pfizer
China - Beijing - Beijing
8d
Lead the Medical Affairs Team to develop post-marketing medical strategies, improve healthcare environments, and maximize Pfizer products' medical value for patients and society.
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Director, Regulatory Strategist
Viatris
Northern Cross, Dublin, Ireland
8d
Develop and implement global regulatory strategies for complex pharmaceutical products, leading regulatory teams and managing interactions with Health Authorities to ensure product development and approval.
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Executive Medical Director, Regional Medical Affairs, CEEM Region
Vrtx
Munich, Germany
8d
Executive Medical Director leading regional Medical Affairs strategy, product launches, and cross-functional alignment for Vertex in the CEEM region.
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Expert Scientific Writer
Sanofi
Hyderabad, IN
8d
Create complex and specialized medical education and publication content for the pharmaceutical industry, managing the end-to-end development process and coaching junior writers.
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Medical Information Specialist / Senior Specialist
Baxter
Warsaw, Masovian, PL
PLN 136k
8d
Deliver high-quality scientific and medical support to healthcare professionals and internal stakeholders across Western Europe, ensuring accurate responses and compliance.
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Medical Communications & Content
Pfizer
Japan - Tokyo
8d
Drive local medical channel content strategy for Pfizer medicines in Japan, adapting global content and developing local assets to optimize engagement with healthcare professionals and patients.
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Customer and Events Manager
Biibhr
Madrid, Spain
8d
Leads and orchestrates Biogen's participation in ex-US international congresses and prioritized external events, managing end-to-end execution from planning to post-event assessment.
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Associate Director, Global Immunology & Cardiovascular Medical Communications (Rheumatology)
Bristolmyerssquibb
Princeton - NJ - US
$156k–$188k
8d
Strategy and execution of medical communication plans for rheumatology to disclose data on scientific and health economic value of BMS products to inform Healthcare Providers, Patients, and Payers.
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Healthcare Content Writer
Highmarkhealth
Pittsburgh PA, 15222, PAP, Penn Avenue Place, US
8d
Develop, write, and edit clinical and healthcare content for client-facing RFI/RFP responses to optimize strategic messaging and support business acquisition.
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CTA Submission Manager
Novartis
London (The Westworks), GB
£48k–£88k
8d
Manage regulatory activities for clinical trial applications across an assigned portfolio, ensuring alignment with regulatory requirements and securing timely approvals.
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Sr. Associate, Promotional Regulatory Affairs Specialist, ASIA (Japanese Speaker)
Alcon
Selangor, Malaysia
8d
Ensuring compliance of promotional and advertising materials with global, regional, and local regulatory requirements for life sciences products.
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Associate Director, Corporate Affairs Poland
Bms
Warsaw - PL
PLN 319k–PLN 387k
8d
Execute end-to-end Corporate Affairs activities (Drug Development, GPS, Commercial and Science Communications) for Poland, covering external media relations, brand reputation, disease awareness, and internal employee engagement.
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Associate Director, US Medical Promotional Review Scientist, Neuroscience
Bms
Princeton - NJ - US
$156k–$188k
8d
Ensure medical accuracy and scientific validity of promotional and non-promotional materials for Neuroscience brands, serving as a strategic partner to marketing and commercial teams.
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Sr. Medical Director, Germany
Acadia Pharmaceuticals
Munich, Bavaria, Germany
8d
Lead the development and execution of the local medical affairs strategy for RETT syndrome in Germany, managing the medical budget and collaborating with MSLs, KOLs, and patient advocacy groups.
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Master Class - Business Consultant - Life Sciences Consulting
Veeva
France - Paris
€60k
8d
Early-career professionals pivot into Life Sciences Consulting through a structured Master Class Program to accelerate drug development and commercialization.
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