Current jobs related to Medical Affairs Specialist - Montreal, Quebec - Otsuka Canada Pharmaceutical Inc


  • Montreal, Quebec, Canada AbbVie Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Medical Affairs Coordinator to join our team at AbbVie. As a Medical Affairs Coordinator, you will be responsible for managing departmental events, projects, and administrative tasks.Key ResponsibilitiesEvent ManagementCoordinate yearly Global/Area staff visits to Canada.Responsible for general...


  • Montreal, Quebec, Canada Pharmascience Inc. Full time

    Regulatory Affairs SpecialistPharmascience Inc. is seeking a highly skilled Regulatory Affairs Specialist to join our team.The successful candidate will be responsible for ensuring the timely and compliant maintenance of products and participating in various regulatory projects with corporate partners in Europe.Key Responsibilities:Assume responsibility for...


  • Montreal, Quebec, Canada Pharmascience Inc. Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Pharmascience Inc. The successful candidate will be responsible for ensuring the timely and compliant maintenance of products and participating in various regulatory projects with corporate partners in Europe.Key ResponsibilitiesAssume responsibility for the...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada Pharmascience Full time

    Job Title: Spécialiste affaires règlementaires, chimie et fabricationThe Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving collaboration and...


  • Montreal, Quebec, Canada GlaxoSmithKline Full time

    Job Summary:We are seeking a highly skilled Medical Science Liaison to join our team at GlaxoSmithKline. As a Medical Science Liaison, you will serve as a key scientific resource for Canadian Hematology/Medical Oncology specialists, providing in-depth scientific information and supporting optimal care for patients with hematological malignancies.Key...


  • Montreal, Quebec, Canada GlaxoSmithKline Full time

    Job Summary:We are seeking a highly skilled Medical Science Liaison to join our team at GlaxoSmithKline. As a Medical Science Liaison, you will serve as a key scientific resource for Canadian Hematology/Medical Oncology specialists, providing in-depth scientific information and supporting optimal care for patients with hematological malignancies.Key...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistSociete Generale's Capital Market Surveillance (CMS) team is seeking a highly skilled Regulatory Affairs Specialist to join our global Compliance department. As a key member of our team, you will be responsible for monitoring security transactions and Firm communications to ensure compliance with applicable policies,...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistAre you passionate about ensuring compliance with regulatory requirements? Do you have a keen eye for detail and a strong understanding of financial regulations? We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at SGS Société Générale de Surveillance SA.Key...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistSociete Generale's Capital Market Surveillance (CMS) team is seeking a highly skilled Regulatory Affairs Specialist to join its global Compliance department. As a key member of the team, you will be responsible for monitoring security transactions and Firm communications to ensure compliance with applicable policies,...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistSociete Generale's Capital Market Surveillance (CMS) team is seeking a highly skilled Regulatory Affairs Specialist to join our global Compliance department. As a key member of our team, you will be responsible for monitoring security transactions and Firm communications to ensure compliance with applicable policies,...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistSociété Générale's Capital Market Surveillance (CMS) team is seeking a highly skilled Regulatory Affairs Specialist to join its global Compliance department. As a key member of the team, you will play a critical role in ensuring the firm's compliance with applicable policies, industry rules, and regulations.Key...


  • Montreal, Quebec, Canada SGS Société Générale de Surveillance SA Full time

    Job Title: Regulatory Affairs SpecialistSociete Generale's Capital Market Surveillance (CMS) team is seeking a highly skilled Regulatory Affairs Specialist to join its global team. As a key member of the Compliance department, you will be responsible for monitoring security transactions and Firm communications to ensure compliance with applicable policies,...


  • Montreal, Quebec, Canada Syneos Health Full time

    Unlock Career Opportunities at Syneos HealthSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success by translating unique clinical, medical affairs, and commercial insights into outcomes.Our Clinical Development model brings together expertise in clinical development, medical affairs, and commercialization to...


  • Montreal, Quebec, Canada Syneos Health Full time

    Unlock Career Opportunities at Syneos HealthSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success by translating unique clinical, medical affairs, and commercial insights into outcomes.Our Clinical Development model brings together expertise in clinical development, medical affairs, and commercialization to...


  • Montreal, Quebec, Canada Pharmascience Full time

    The Regulatory Affairs Specialist, Chemistry and Manufacturing plays a crucial role in ensuring the timely and compliant maintenance of products within the department. This position participates in various regulatory projects with corporate partners in Europe, driving regulatory excellence and compliance.Key Responsibilities:Maintains and ensures regulatory...

Medical Affairs Specialist

3 months ago


Montreal, Quebec, Canada Otsuka Canada Pharmaceutical Inc Full time

Department:
Medical and Regulatory Affairs

Reports To:
Senior Director, Medical Affairs, Nephrology
The role involves supporting Medical Affairs initiatives for the Nephrology product line. This includes providing unbiased, scientifically grounded insights and education regarding the disease landscape and the Nephrology product offerings.

Engagement with healthcare professionals, including key opinion leaders (KOLs) and investigators, is essential to enhance patient care outcomes.


Key Responsibilities:
• Deliver scientific and medical knowledge for Nephrology products, from late-stage development through the entire product lifecycle.
• Contribute strategic scientific and medical insights to the formulation of brand medical strategies and comprehensive brand plans, particularly during product launches.
• Assist in the creation and implementation of medical affairs strategies for Nephrology brands throughout their lifecycle, which encompasses late-phase studies, investigator-initiated trials, data analysis, publications, and other medical initiatives.
• Participate in scientific conferences and meetings to stay informed about advancements in the field.
• Foster relationships with KOLs, investigators, external consultants, and vendors.
• Provide medical insights and scientific evaluations to the brand team, including Medical Information, Pharmacovigilance, Regulatory Affairs, Market Access, and Commercial functions (including reviewing promotional materials).
• Offer medical expertise and scientific training across the brand team.
• Report safety information, product quality issues, and customer feedback in accordance with established procedures.
• Establish a reputation as a reliable medical and scientific resource for opinion leaders, demonstrating expertise in the relevant products, treatment trends, clinical trials, and scientific research.
• Communicate current and emerging clinical research findings to opinion leaders in response to inquiries.
• Identify medical professionals to serve as speakers, consultants, and investigators.
• A PhD or PharmD with over 5 years of experience in the pharmaceutical sector, particularly in Clinical Research and Medical Affairs, is preferred.
• Proven expertise in the Nephrology therapeutic area and the ability to interpret complex scientific data and concepts.
• Excellent communication and presentation skills, with the capability to convey intricate scientific information to diverse audiences.
• A thorough understanding of Canadian pharmaceutical safety reporting and surveillance practices.
• Ability to work autonomously and collaboratively within teams, including cross-functional groups and external networks.
• Strong interpersonal skills, integrity, teamwork capabilities, and a customer-centric approach are essential.
• Awareness of business strategies and the implications of scientific and medical decisions.