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Agent(e), Liaison médicale et scientifique, Immunologie / Medical Scientific Liaison, Immunology

MSD

Toronto

Hybrid

CAD 90,000 - 120,000

Full time

12 days ago

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Job summary

A leading healthcare company is seeking a Medical Scientific Liaison to provide expert medical and scientific communication within the field of Irritable Bowel Disease. This role requires a Pharmacy Doctorate or PhD in Health Sciences and involves engaging with key decision-makers to enhance patient care. Candidates must possess strong interpersonal skills and a solid understanding of the relevant therapeutic area, capable of delivering balanced and insightful data to healthcare professionals. Join us in our commitment to innovation and improving patient outcomes.

Qualifications

  • Pharmacy Doctorate or PhD in Health Sciences required.
  • Strong knowledge of therapeutic area and advanced analytical skills needed.
  • Proven experience in industry preferred.

Responsibilities

  • Engaging in non-promotional peer-to-peer communication with scientific leaders.
  • Representing Medical Affairs at medical events.
  • Responding to requests for medical and scientific information.

Skills

Interpersonal skills
Analysis
Negotiation
Presentation
Project management

Education

Pharmacy Doctorate
PhD Degree in Health Sciences
Doctorate in Medicine

Tools

Office technology

Job description

Qualifications:

Reporting to the Director, Medical Affairs, the Medical Scientific Liaison is a field-based medical professional whose primary responsibility is to engage in non-promotional peer-to-peer communication, using very strong interpersonal skills & provide medical/scientific information to Scientific Leaders and Key Decision Makers based on cutting-edge scientific exchange and services oriented towards the stakeholder’s professional interests & needs.

The Medical Scientific Liaison is responsible for ensuring that they are fully versed in the therapeutic area (mainly Irritable Bowel Disease) and up to date on all major studies, both ongoing and completed, product information on our Company’s and other companies’ relevant therapies, clinical data and relevant pipeline data to provide the most balanced data to Scientific Leaders, Key Decision Makers and the healthcare community to improve patient care.

Roles and responsibilities:

Engaging in non-promotional peer-to-peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers to the extent permitted by law and local regulation, local industry codes, and other provisions of the Field medical standard operating procedure.

Gaining deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in their local geography.

Representing Medical Affairs at local or regional non-promotional Medical events (e.g. Medical Congresses and Symposia) They may collaborate in the coordination of pre-event scientific information and post-event scientific summaries.

Responding to unsolicited requests for medical, scientific, pipeline or marketed product information or indications from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials.

Responding (one-to-one) to unsolicited requests for information on company research and/or grant activities by directing Scientific Leaders or Key Decision Makers to appropriate company resources for grants, sponsored clinical trial involvement, our Company’s Investigator Study Program, and outcomes research.

Participating in Scientific Advisory Board Meetings or Expert Input Forums when there is a defined role.

Participating in the development of Medical Affairs Plans and implementation of activities identified in the Medical Affairs Plans.

At Global Clinical Trials Organization, or Center for Observational and Real World Research personnel request, supporting the identification of potential study investigators for sponsored study

Qualifications:

Pharmacy Doctorate; PhD Degree in Health Sciences (preferably in related disease area) or Doctorate in Medicine.

Industry experience and/or expertise in the related therapeutic area is preferred.

Good knowledge of therapeutic area (both basic and clinical literature).

Demonstrated ability to acquire and maintain product, disease and competition knowledge.

Strong interpersonal skills.

Strong knowledge of Company policies, procedures, industry standards, as well as laws and regulations.

Ability to analyze and understand local community of practice.

Ability to comprehend and integrate complex scientific concepts (e.g. proteomics, metabolic networks or molecular mechanisms of disease).

Advanced knowledge of Office technology and related software.

Advanced Analysis, Planning, Implementation and Control skills.

Advanced negotiation, presentation, and facilitation skills.

Advanced project management skills.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Job Description

Relevant du directeur, médécines spécialisées, Affaires médicales, l’agent de liaison médicale et scientifique est un professionnel médical sur le terrain dont la responsabilité principale consiste à communiquer d’égal à égal de façon non promotionnelle et à utiliser son savoir-faire social poussé pour offrir des renseignements médicaux et scientifiques aux leaders scientifiques ou les décideurs clés basés sur un échange et des services scientifiques de pointe favorisant les intérêts et les besoins professionnels du partenaire professionnel.

L’agent de liaison médicale et scientifique s’assure qu’il connaît à fond le domaine thérapeutique (immunologie et Syndrôme du Colon Irritable) et toutes les études importantes tant en cours que terminées, les renseignements sur les produits concernant les thérapies pertinentes de Notre Entreprise et autres sociétés, les données cliniques et les données sur les produits en développement pertinentes pour offrir les données les plus équilibrées aux les leaders scientifiques, aux décideurs clés et au secteur de la santé pour améliorer les soins aux patients.

Rôles et responsabilités:

  • Faire des échanges non promotionnels d’égal à égal de renseignements médicaux et scientifiques avec les leaders scientifiques ou les décideurs clés dans la mesure où la loi et la réglementation locales, les codes sectoriels locaux et les autres dispositions du mode opératoire normalisé médical sur le terrain le permettent.

  • Obtenir des intuitions profondes sur les maladies, le domaine thérapeutique et les besoins en matière de soins de santé, les lacunes dans les données et les défis liés à la géographie locale.

  • Représentant les Affaires médicales à des événements médicaux locaux ou régionaux non promotionnels (p. ex., congrès ou symposiums médicaux), collaborer à la coordination des renseignements scientifiques avant l’événement et aux résumés scientifiques après l’événement.

  • Répondre aux demandes non sollicitées de renseignements médicaux ou scientifiques ou sur les produits en développement ou sur le marché ou aux indications des leaders scientifiques ou les décideurs clés au moyen de matériel scientifique approprié et approuvé.

  • Répondre (seul à seul) aux demandes non sollicitées de renseignements sur les recherches de la société et/ou les activités en matière de subventions en aiguillant les leaders scientifiques ou les décideurs clés vers les ressources appropriées de la société pour les subventions, la participation à des essais cliniques commanditée, le programme d’études de chercheurs de Notre entreprise et les recherches sur les résultats.

  • Participer aux réunions du conseil consultatif scientifique ou aux forums de discussions d’experts quand il y a un rôle défini.

  • Participer aux plans des Affaires médicales et à la mise en œuvre d’activités indiquées dans les plans des Affaires médicales.

  • À la demande des Opérations mondiales liées aux essais cliniques ou du Centre mondial d’études d’observation et d’études de vie réelle, appuyer l’identification d’investigateurs de l’étude potentiels pour l’étude commanditée.

Qualifications:

  • Diplôme de doctorat en pharmacie (Pharm. D.); doctorat (PhD) en sciences de la santé (lié au domaine de la maladie de préférence) ou en médecine (MD).

  • Expérience en industrie et/ou expertise dans le domaine thérapeutique connexe de préférence.

  • Expérience pharmaceutique ou l’équivalent, de préférence avec des spécialistes universitaires et/ou des chefs de communauté.

  • Bonnes connaissances du domaine thérapeutique (documentation de base et clinique).

  • Capacité démontrée à acquérir et à entretenir des connaissances sur les produits, les maladies et les compétiteurs.

  • Compétences linguistiques : Anglais

  • Solides compétences en relations interpersonnelles.

  • Compétences en gestion des budgets.

  • Très bonne connaissance des politiques et des procédures de la société ainsi que des normes, lois et règlements de l’industrie.

  • Capacité à analyser et à comprendre la communauté locale de la pratique.

  • Capacité à comprendre et à assimiler des concepts scientifiques complexes (p. ex., la protéomique, les réseaux métaboliques ou les mécanismes moléculaires des maladies).

  • Connaissance avancée de la technologie et des logiciels Office.

  • Compétences avancées en analyse, en planification, en mise en œuvre et en suivi.

  • Compétences avancées en négociation, en présentation et en animation.

  • Compétences avancées en gestion de projet.

Territoire: Ontario

Nous sommes fiers d'être une entreprise qui embrasse la valeur de rassembler des personnes diversifiées, talentueuses et engagées. La façon la plus rapide d’innover est de rassembler des gens de diverses opinions dans un environnement inclusif. Nous encourageons nos collègues à remettre en question avec respect les problèmes de réflexion et d’approche de l’un et de l’autre. Nous sommes un employeur souscrivant au principe de l’égalité d’accès à l’emploi et nous sommes déterminés à favoriser un milieu de travail inclusif et diversifié.

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description:

Reporting to the Director, Medical Affairs, the Medical Scientific Liaison is a field-based medical professional whose primary responsibility is to engage in non-promotional peer-to-peer communication, using very strong interpersonal skills & provide medical/scientific information to Scientific Leaders and Key Decision Makers based on cutting-edge scientific exchange and services oriented towards the stakeholder’s professional interests & needs.

The Medical Scientific Liaison is responsible for ensuring that they are fully versed in the therapeutic area (mainly Irritable Bowel Disease) and up to date on all major studies, both ongoing and completed, product information on our Company’s and other companies’ relevant therapies, clinical data and relevant pipeline data to provide the most balanced data to Scientific Leaders, Key Decision Makers and the healthcare community to improve patient care.

Roles and responsibilities:

  • Engaging in non-promotional peer-to-peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers to the extent permitted by law and local regulation, local industry codes, and other provisions of the Field medical standard operating procedure.

  • Gaining deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in their local geography.

  • Representing Medical Affairs at local or regional non-promotional Medical events (e.g. Medical Congresses and Symposia) They may collaborate in the coordination of pre-event scientific information and post-event scientific summaries.

  • Responding to unsolicited requests for medical, scientific, pipeline or marketed product information or indications from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials.

  • Responding (one-to-one) to unsolicited requests for information on company research and/or grant activities by directing Scientific Leaders or Key Decision Makers to appropriate company resources for grants, sponsored clinical trial involvement, our Company’s Investigator Study Program, and outcomes research.

  • Participating in Scientific Advisory Board Meetings or Expert Input Forums when there is a defined role.

  • Participating in the development of Medical Affairs Plans and implementation of activities identified in the Medical Affairs Plans.

  • At Global Clinical Trials Organization, or Center for Observational and Real World Research personnel request, supporting the identification of potential study investigators for sponsored study

Qualifications:

  • Pharmacy Doctorate; PhD Degree in Health Sciences (preferably in related disease area) or Doctorate in Medicine.

  • Industry experience and/or expertise in the related therapeutic area is preferred.

  • Good knowledge of therapeutic area (both basic and clinical literature).

  • Demonstrated ability to acquire and maintain product, disease and competition knowledge.

  • Language requirements: English

  • Strong interpersonal skills.

  • Budget management skills.

  • Strong knowledge of Company policies, procedures, industry standards, as well as laws and regulations.

  • Ability to analyze and understand local community of practice.

  • Ability to comprehend and integrate complex scientific concepts (e.g. proteomics, metabolic networks or molecular mechanisms of disease).

  • Advanced knowledge of Office technology and related software.

  • Advanced Analysis, Planning, Implementation and Control skills.

  • Advanced negotiation, presentation, and facilitation skills.

  • Advanced project management skills.

Territory: Ontario

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

50%

Flexible Work Arrangements:

Remote

Shift:

Not Indicated

Valid Driving License:

Yes

Hazardous Material(s):

No

Required Skills:

Preferred Skills:

Job Posting End Date:

05/30/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

About the company

Merck & Co., Inc.

Notice

Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at accessibility@talentify.io or 407-000-0000.

Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility.

An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: www.talentify.io/bias-audit-report . NYC applicants may request an alternative process or accommodation at aedt@talentify.io or 407-000-0000.

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