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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.
A pipeline Medical Science Liaison (pMSL) is a key member of the Canadian Oncology Medical Affairs team. This field-based role focuses on interacting with, and supporting the needs of, investigators participating in our studies. Pipeline MSLs work to communicate information and facilitate scientific dialogue about AbbVie’s investigational products and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable Canadian laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures (see Note 3, below) and accepted standards of best practice.
Pipeline MSLs serve to enhance the scientific credibility of AbbVie with established and emerging clinical investigators as well as key scientific institutions and collaborative study groups, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of request for scientific and medical information. Pipeline MSLs also participate in close partnership with Canadian-based Clinical Site Monitoring (CSM) staff in the initiation, oversight, and follow-up of clinical studies. They also interface with other key members of the affiliate medical department - for example: Therapeutic Area Leads, Medical Advisors, Clinical Research Associates, and other functions such as Health Economics and Outcomes Research, Market Access and others as appropriate – relevant to the therapeutic area for which the pMSL has responsibility and work collaboratively and cross-functionally with other in-field team members while retaining functional independence. They maintain a high level of scientific knowledge to ensure credible dissemination of scientific information and informed scientific dialogue with key external stakeholders.
Core Responsibilities
- Ensure a strong medical and scientific presence for AbbVie in investigational sites and key scientific centers by facilitation of clinical research and of interventional phase 1-3 trials with AbbVie drugs, while supporting requests for medical and scientific information on products or areas of therapeutic interest to Abbvie.
- Establish and maintain a close working relationship with CSM staff and partner in facilitating the initiation and conduct of prioritized AbbVie-led clinical trials.
- Provide scientific and technical leadership to ensure professional and credible relationships with investigators.
- Consult with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the investigator or referring sites.
- Act as the point of contact with thought leaders to facilitate investigator-initiated study (IIS) ideas with AbbVie pipeline assets and requests for support to the local and global medical teams as appropriate.
- Deliver credible presentations on scientific matters in the disease area of responsibility and about AbbVie’s pipeline to investigators in Abbvie-sponsored interventional research.
- Participate in the selection process to identify appropriately qualified external experts the Company would wish to engage in collaborative efforts – such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.
- Identify opportunities for R&D collaborations with key institutions and thought leaders and liaise with the Search & Evaluation team and Discovery or Clinical Development teams to facilitate further assessment.
- Facilitate medical and scientific field intelligence – for example, maintain a list of investigators/potential investigators within a given TA, understand competitive research activities in active or planned study sites, generate insights from investigators on challenges and opportunities for AbbVie-sponsored clinical trials – and communicate, where appropriate, within the Company.
- Attend relevant scientific meetings and Conferences.
- Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.
- For countries involved in the 1-7-5 early touchpoint process: provide insights on the current clinical practice, facilitate identification of tier 1 external experts and provide scientific input into the future clinical development program for AbbVie’s pipeline assets.
- Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.