Medical Science Liaison supporting AbbVie’s Quebec medical affairs team. Building healthcare expert relationships and communicating scientific evidence across ophthalmology initiatives.
About the role
- Medical Science Liaison for Rheumatology in Vancouver, Calgary, Edmonton. Engaging with healthcare professionals and leading scientific discussions in the field.
Responsibilities
- Maintaining up-to-date scientific expertise with regular attendance at key scientific/clinical/economic conferences, training sessions and preceptorships to translate data into applicable knowledge and communication platform.
- Disseminating, reviewing and presenting clinical and scientific data in a balanced, unbiased manner, to key opinion leaders and other HCPs, in group and one-on-one settings.
- Building strong relationships with HCPs based on scientific credibility.
- Developing scientific communication materials (slide presentations) for dissemination to HCPs through contacts and meetings and provide congress support.
- Ensuring a regional scientific leadership strategy via credible and informed scientific dialogue with KIs.
- Leading/participating in medical and scientific forums (e.g., ad boards and medical education events) where KIs are involved.
- Supporting phase IIIB/IV local and global clinical development program
- Being a critical contributor to site identification, patient enrollment, and follow-up visits.
- Assisting in the interpretation of results, post-hoc analyses, and research collaboration with investigators
- Supporting investigator-initiated studies by fielding and assessing research requests, aligning investigator interests with JJIM’s research needs, and engaging investigators to ensure the successful execution and satisfactory completion of studies.
- Analyzing data – new and post hoc – to develop insights and contribute to publications as appropriate.
- Providing expert clinical consultation and support to business partners (e.g. Access, Medical Education, Sales and Marketing etc. as appropriate).
- Partnering and collaborate with in-house business partners to facilitate ongoing exchange of clinical information.
- Providing regional medical perspective to influence the integrated Medical Affairs plan which complements the ILCP (Integrated Lifecycle) plans.
- Supporting the Medical Science publication plan.
Requirements
- A minimum of a University degree in science or health-related field at a minimum with significant therapeutic-area experience is required
- MD and/or PhD, PharmD preferred
- Have a proven ability to learn quickly, assimilate and distill large amounts of information and build and maintain relationships
- Strategic thinking and positive track record of flawless execution
- Proven ability to effectively communicate information to KIs, as well as non-experts
- Ability to put data into perspective and communicate it concisely
- Demonstrated critical thinking, strong project management skills and ability to impact decision making with relevant stakeholders
- Business acumen, including prioritization skills and big picture orientation
- Scientific knowledge, curiosity, familiarity and interest to keep abreast of scientific trends within the therapeutic area
- Demonstrated ability to take initiative, prioritize tasks, and follow through in a field-based role
- Working knowledge of Microsoft Office and other relevant software programs
- Ability to travel nationally as well as internationally
- Drivers license and valid passport are required.
- Ability to travel up to 70% of the time (customer-facing position)
- Overnight travel may be required as much as 1-2 times per week on average, depending upon region covered
- Minimum of 2 years business experience in the pharmaceutical industry, which can be balanced against a strong clinical and/or scientific background in a relevant therapy area
- proven track record of contribution to commercial, medical and/or clinical development strategies
- Knowledge of the therapeutic area of interest is an asset, should have the ability to acquire expertise in other therapeutic areas and products, depending on pipeline and/or changing business priorities
- Demonstrated experience of managing clinical/ scientific programs with a high degree of autonomy, including successfully managing significant programs from study concept to publication
- Strong knowledge of GCP, IMC code and Healthcare Compliance policies and procedures
- Familiarity with working in an environment guided by SOPs
Benefits
- N/A
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