Medical Advisor, Psychiatry

at  AbbVie

Company Description
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
Joining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients’ lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada.
When choosing your career path, choose to be remarkable.
AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, vision care, virology, women’s health , and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio.
We have an opportunity for a Medical Advisor to join our Medical Affairs team. This position is National in scope and based in Montreal. This role reports to the Therapeutic Area Lead for Therapeutic Area.
As Medical Advisor, you will provide medical and scientific support to the clinical research department and collaborate in clinical operation activities. The Medical Advisor develops strategic plans that are aligned with the brand plan and closely collaborates and supports different groups in the organization.

Key Responsibilities:

• Develop a medical strategy within the brand team and execute as defined in the brand plan.
• Support clinical study feasibility, site mapping, identification and participation and provide support with resolving any pending issues with the study sites.
• Review new clinical study protocols and investigator-initiated research proposals.
• Liaise with local commercial groups, global project teams, investigators and external experts through regular review of ongoing initiatives and the tactical implementation of plans.
• Provide scientific and medical support for ongoing projects.
• Monitor and review scientific literature on AbbVie products and competition.
• Serve as a scientific affairs expert for the product.
• Serve as liaison between the Medical Division and the commercial groups on the respective therapeutic areas.
• Ensure regulatory compliance in all studies undertaken.
• Diligently manage and allocate resources by ensuring that all projects are carried out within approved budgets and that expected results are delivered.
• Support the integration of new products into AbbVie’s portfolio.
• Lead the evidence generation plan based on identified data gaps.

Qualifications

Key Responsibilities:

• Develop a medical strategy within the brand team and execute as defined in the brand plan.
• Support clinical study feasibility, site mapping, identification and participation and provide support with resolving any pending issues with the study sites.
• Review new clinical study protocols and investigator-initiated research proposals.
• Liaise with local commercial groups, global project teams, investigators and external experts through regular review of ongoing initiatives and the tactical implementation of plans.
• Provide scientific and medical support for ongoing projects.
• Monitor and review scientific literature on AbbVie products and competition.
• Serve as a scientific affairs expert for the product.
• Serve as liaison between the Medical Division and the commercial groups on the respective therapeutic areas.
• Ensure regulatory compliance in all studies undertaken.
• Diligently manage and allocate resources by ensuring that all projects are carried out within approved budgets and that expected results are delivered.

• Support the integration of new products into AbbVie’s portfolio.Lead the evidence generation plan based on identified data gaps.

EDUCATION/EXPERIENCE REQUIRED:

• Doctorate, MD or Pharm D is required.
• Relevant experience with solid knowledge of the biotech/pharmaceutical industry.
• General knowledge on drug/device development and clinical research in ophthalmology therapeutic area (minimum of three to five years).
• Relevant background and experience in Ophthalmology Dermatology therapeutic area (minimum of two to three years).
• Previous scientific experience in customer-facing role in the healthcare industry.
• Ability to prepare and deliver high quality presentations and/or interpretation of scientific or clinical research publications.
• Ability to think and plan strategically (work plans, activities, timetables, targeting) and operating with execution excellence.
• Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.
• Knowledge of all aspects of drug development and local regulations, including regulations of promotional materials.

ESSENTIAL SKILLS & ABILITIES:

• Advanced French and English language proficiency (oral and written).
• Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
• Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
• Travel required at least 20-30% of the time.
• Valid driver’s license and passport.

KEY LEADERSHIP COMPETENCIES:

• In-depth understanding and execution of meaningful strategies and data-based business decisions.
• Demonstrated organizational and analytical skills to set priorities, monitor progress towards goals, and track data, information and activities. Effectively manage budgets to deliver on fiscal commitments.
• Display sound business judgment (having an executive leadership mindset to assess local market and set direction). Ability to predict contingent outcomes from both a customer and competitive perspective.
• Possess knowledge of AbbVie’s therapeutic areas and products to coach team members, who engage in scientific interactions with key stakeholders, external experts, and medical associations.
• Effectively communicate and collaborate with other team members to ensure alignment on plans.
• Demonstrate organizational and analytical skills.
• Ability to foster teamwork by working cooperatively and effectively with others to resolve, problems, and make decisions that enhance organizational effectiveness.
• Ability to make decisions independently and with appropriate input.
• Ability to take feedback constructively and consider the viewpoints of others.
• Demonstrate leadership approach to unite and motivate others to achieve results that are in the best interest of the region and organization.
• Demonstrate ability to be versatile and optimistic in a changing work environment while maintaining effectiveness and efficiency in a matrix environment.

AbbVie strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the following requirement, advanced amount of knowledge of English / Fluency in English is an essential requirement for the position of Medical Advisor including, but not limited to, for the following reasons:

• English speaking employees outside the province of Quebec.
• English speaking clients outside the province of Quebec.
• Anglophone region outside the province of Quebec.

AbbVie is an equal opportunity employer and encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.htm

Key Responsibilities:

• Develop a medical strategy within the brand team and execute as defined in the brand plan.
• Support clinical study feasibility, site mapping, identification and participation and provide support with resolving any pending issues with the study sites.
• Review new clinical study protocols and investigator-initiated research proposals.
• Liaise with local commercial groups, global project teams, investigators and external experts through regular review of ongoing initiatives and the tactical implementation of plans.
• Provide scientific and medical support for ongoing projects.
• Monitor and review scientific literature on AbbVie products and competition.
• Serve as a scientific affairs expert for the product.
• Serve as liaison between the Medical Division and the commercial groups on the respective therapeutic areas.
• Ensure regulatory compliance in all studies undertaken.
• Diligently manage and allocate resources by ensuring that all projects are carried out within approved budgets and that expected results are delivered.
• Support the integration of new products into AbbVie’s portfolio.
• Lead the evidence generation plan based on identified data gaps

Key Responsibilities:

• Develop a medical strategy within the brand team and execute as defined in the brand plan.
• Support clinical study feasibility, site mapping, identification and participation and provide support with resolving any pending issues with the study sites.
• Review new clinical study protocols and investigator-initiated research proposals.
• Liaise with local commercial groups, global project teams, investigators and external experts through regular review of ongoing initiatives and the tactical implementation of plans.
• Provide scientific and medical support for ongoing projects.
• Monitor and review scientific literature on AbbVie products and competition.
• Serve as a scientific affairs expert for the product.
• Serve as liaison between the Medical Division and the commercial groups on the respective therapeutic areas.
• Ensure regulatory compliance in all studies undertaken.
• Diligently manage and allocate resources by ensuring that all projects are carried out within approved budgets and that expected results are delivered.
• Support the integration of new products into AbbVie’s portfolio.Lead the evidence generation plan based on identified data gaps