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Medical Science Liaison (Quebec, Atlantic, Canada)

Medical Science Liaison (Quebec, Atlantic, Canada)

Sumitomo Pharma America, Inc.Québec, Canada, CA
30+ days ago
Job type
  • Full-time
Job description

Medical Science Liaison (Quebec, Atlantic, Canada)Medical Science Liaison (Quebec, Atlantic, Canada)We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Medical Science Liaison, Urology (Quebec, Atlantic or as assigned). This position will be reporting to the Executive Director, Scientific Affairs.Job Duties & ResponsibilitiesProvide balanced, fair, objective scientific information and education to healthcare professionals (including HCPs, academic institutions, payors, patient organizations), and internal colleagues as required by scientific or business needs.Identify, build, and maintain professional and credible relationships with Key Opinion Leaders (KOLs), in academic and clinical practices.Provide scientific and technical support for KOLs and academic centres to ensure access to current medical and scientific information on company products and areas of therapeutic interest.Develop strategic thinking and geographical management skills in building and executing territory plans in alignment with regional and national plans.Respond to unsolicited requests from external customers for scientific information and education on the disease state and the safe and effective use of the company’s marketed products or products in development.Support Market Access colleagues, including presentations to reimbursement bodies as requested.Develop awareness and understanding of the competitive landscape, clinical strategies, and other developments relevant to corporate objectives with internal stakeholders.Develop and build on scientific and business acumen and demonstrate operational activities including timely completion of assigned tasks, documentation requirements, milestones, and required training.Represent and support the company at scientific meetings including congresses, symposia, poster sessions or other venues and interpret and report findings / action items to relevant internal stakeholders.Participate in training and assessment of thought leaders for participation in speaker bureau programs.Effectively collaborate with cross functional partners in a constructive fashion to ensure healthy team dynamic and a positive and enthusiastic work environment.Ensure all activities and interactions are compliant with all applicable local, global and national laws, regulations, guidelines, code of conduct, Company policies and SOPs.Foster accountability via documentation of field-based activities and providing special project updates.Professional Experience / Qualifications : Advanced degree preferred (e.G., MD, PhD); other degrees will be considered dependent on working knowledge and experience in the designated therapeutic area.Bilingual (English / French) required.Demonstrated combination of analytical, organizational, time management and interpersonal skills.Ability to understand and effectively communicate scientific and medical information.Solid knowledge of the pharmaceutical environment and excellent skills to build relationships with key stakeholders.Understanding of health economics / outcomes research and interpretation of results.Strong commitment to compliance with IMC codes and company policies and procedures and to scientific quality and integrity.Must have excellent customer-service orientation, high degree of professionalism.Ability to multi-task under limited direction and on own initiative while working under tight deadlines.Daily demonstrates a positive, ‘can do’ and service-oriented attitude; detail-oriented with a commitment to accuracy.Self-motivated, with initiative and the ability to take ownership of, and follow through with, specific tasks.Demonstrated proficiency in MS Office (Outlook, Word, Excel, PowerPoint).Excellent verbal and written communication skills, as the position will interface with key opinion leaders and employees.Proven team player - work well with team members to accomplish common goals.Other RequirementsAvailability to travel and to drive. Significant travel is required (>

70%) with overnight stays.Confidential DataAll information (written, verbal, electronic, etc.) that an employee encounters while working at Sumitomo Pharma Canada, Inc. is considered confidential.ComplianceAchieve and maintain compliance with all applicable regulatory, legal and operational rules and procedures by ensuring that all plans and activities for and on behalf of Sumitomo Pharma Canada, Inc. are carried out with the best industry practices and the highest ethical standards.Mental / Physical RequirementsFast-paced environment requires handling multiple demands. Must be able to exercise appropriate judgment, as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a laptop / PC / iPad for extended periods of time.Sumitomo Pharma Canada, Inc. provides a robust benefit plan including established vacation, RRSP and TFSA options, and comprehensive health benefits, details of which will be provided upon successful hiring.Disclaimer : The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.#J-18808-Ljbffr

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Medical Science Liaison • Québec, Canada, CA