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Medical Affairs’ Search for Meaning

Publication
Article
Pharmaceutical ExecutivePharmaceutical Executive-10-01-2018
Volume 38
Issue 10

The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.

The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes 

 

"Between stimulus and response there is a space. In that space is our power to choose our response. In our response lies our growth and our freedom.”

 

This quote from Victor Frankl perfectly reflects the mindset of great medical affairs teams in pharmaceutical companies at the moment. The time is now, and it is for the medical affairs function to determine if it wants to have a bright future and be a true partner and a leading value driver.

For pharma organizations in the past, the commercial function was the only lead in setting and driving the strategy. Medical affairs, in addition to the license-to-operate function, provided mostly on-demand medical information services, as well as support on an ad hoc basis in key external experts’ engagement and internal and external medical education. The key performance indicators (KPIs) and the resulting perceived value were related to these support activities, and were expressed in inconsequential metrics, including but not limited to the number of visits to external experts and the number of evidence-generation activities and publications.

Redefined role

Innovative specialty and ultra-specialty pharma companies have recently invested heavily in expanding the medical affairs function, due to the complexity of therapeutic areas and medicines, with more and more medical affairs colleagues working in the field, while at the same time improving the quality and impact of those medical teams. They, in essence, are internal experts employed by the company. This dynamic changed the scope and value of medical affairs dramatically. From our perspective, however, the purpose of being (raison d’etre) for medical affairs is to ensure the best patient outcomes via shaping the practice of medicine through evidence generation and scientific exchange activities, and enhancing patient access to the best available treatment by demonstrating its value to payers, physicians, and patients.

The only way to achieve best patient outcomes for the medical affairs function is a true peer-to-peer partnership with external experts, scientific societies, academic institutions, and research groups, as well as the entire medical community involved in patient care. In order to become a partner, you need to be considered as a peer in a specific therapeutic area.

But what can make a good pharma medical affairs professional a peer to an external expert, in addition to having in-depth scientific, clinical, and medical knowledge in the relevant therapeutic area and medicine(s)? The answer is an ability to understand patients’ needs, think across therapeutic areas, assess clinical value, analyze risk versus benefit, and exploit technological advances.2

In addition, a sustainable, trustful, and successful partnership is only possible in cases where external experts engage with medical affairs professionals as peers; have confidence in our unbiased data; look to us for our medical expertise and scientific reference; and want to involve us and collaborate in evidence generation, policy shaping, regulatory, and patient access activities, as well as listen to us at scientific forums, because we own the science they value. Medical affairs has a huge ethical responsibility in creating this trusted and sustained partnership. 

Insights unlocked

Medical affairs is the only function to systematically provide the physician’s perspective to the drugmaker.The medical science liaisons (MSLs) bring these insights back into the company, based on a peer-to-peer discussion. By listening carefully to the medical community, the medical strategy will be adapted with the patient outcome as the sole goal. Indeed, the best medical professionals, physicians, and medical professionals of pharma companies alike, always have the patients’ needs at the forefront of their minds and actions. They always see the disease through the patients’ eyes and help the company to transform patients’ needs into their deliverables. This is non-negotiable and medical affairs should proudly represent this point of view.

In turn, higher investment in headcounts and quality, with a specific focus on external scientific exchange and education activities (by MSLs), the quality of the output, and the greater responsibility regarding evidence generation activities to fill evidence gaps has led to an increased demand from the business to measure the value of medical affairs.

Many companies developed KPIs, measuring the number of external engagements with targeted experts per quarter, the number of publications in peer-reviewed journals based on evidence-generation activities, and the number of medical education events or advisory boards. These numbers are extremely important for internal

tracking and benchmarking but do not fully reflect the real value of the leadership role of medical affairs. They, instead, result in a “KPI trap,” where medical affairs produces ever-bigger dashboards that do not reflect the true value, leading to a misunderstanding and a perception of medical affairs as a cost center. 

That returns us to the pragmatic challenge of the medical affairs function, having to show the value and impact to the business first, and, next, to the patients, physicians, and payers. Relevant value measurements should be related to mainly two deliverables and supplement traditional numerical KPIs.

  • Access to our medicines for the right patient at the right time.

  • Shaping medical practice based on evidence generated in collaboration with external experts and payers to optimize patient treatment and outcomes.

 

 

Which relevant measurements should be considered in the future? With respect to quantitative and qualitative KPIs, we do not think it is an either/or question. Great MSLs and medical teams will need both quantity and quality. It doesn’t matter how good your science is; if you are not meeting regularly with the key external experts (KEEs), your impact will be limited. We believe “traditional KPIs” such as number of publications and advisory boards or number of field visits and interactions per MSL should still be measured and put into a dashboard to understand and benchmark the quantitative output of what we do; but these, what we will now define as “traditional numerical KPIs,” should not be used as the justification of the medical affairs function and its activities.

Value and impact measurements-like documented examples of change in medical practice; inclusion of a medicine in a protocol or formulary based on trusted evidence and confidence; independent external expert feedback of the value of the medical affairs function-are the new ways forward as they better reflect the desired outcomes for patients. 

By implementing this approach, the need and request to justify the existence of medical affairs is no longer necessary, because the value and impact on patients’ outcomes as the ultimate goal of the pharmaceutical company will be clear and obvious.

The value and impact measurements are the result of the overall value proposition framework of medical affairs. In our view the medical affairs value proposition framework consists of five interrelated elements:

  • Excel in pharmacovigilance and regulatory license-to-operate (LTO) activities.

  • Shape the practice of medicine by evidence generation and building on this through scientific exchange activities, with the objective to develop strong value propositions. These activities, as well as the medical affairs strategy in general, need to be highly relevant to the current and future business and always should stay two steps ahead on pre-launch planning to lead the rest of the company.

  • Drive strategy by science and insights. The medical affairs function ensures the incorporation of medical practice and patient insights into the drug manufacturer’s strategy.

  • Enhance patient access to the best treatment available by demonstrating value to payers, physicians, and patients.

  • Provide a talent pipeline for evolving tasks across the company.

Pharma companies often unintentionally create “silos” within their organizations, where medical affairs, sales and marketing functions, and clinical research don’t share critical data in time, and only rely on loosely organized cross-functional teams. When this is the case, medical affairs does not get the information it needs to develop productive external relationships. Companies must include medical affairs as a full partner in all stages of the drug life cycle, from R&D to commercialization, and should grant medical affairs full access to essential information from all parties involved in this cycle.Only in this way, can this function truly make a difference, create an equal playing field, and address patient and physician needs.

Trusted exchange    

Imagine a world where pharma companies have a real peer-to-peer discussion based on mutual trust coming from studies and data with the patient in mind. This is the direction the life sciences industry is going. Medical affairs owns this space of building trust. There are no multiple truths. The data and the science speak for themselves and should lead to a consensus between the larger medical world and the pharma industry.

Innovative organizations do not sell drugs as an endpoint and a goal by itself, but are leaders and indispensable partners in improving patients’ lives through well-informed physicians, based on a broad scientific consensus. Since patients are not quantifiable, numerical KPIs as sole measurements of medical affairs’ value are something of the past. 

Patient outcomes should become the only measurement on which medical affairs and, as a consequence, the larger pharmaceutical company should be judged in the future. Medical affairs is in the unique position to lead this evolution. 

 

Alexander Bedenkov is Vice President, Medical; Filip Surmont is Medical Director,  Cardiovascular and Metabolic Disease; and Maarten Beekman is Medical Director,  Respiratory, Inflammation, and AutoImmune; all with AstraZeneca International Region

 

References

1. Frankl, V. E. Man’s search for meaning. Beacon Press, 2006 

2. Managing talent in the medical affairs function: Creating value through a strengths-based approach. McKinsey & Company, and Korn/Ferry International, 2013. https://www.kornferry.com/institute/download/view/id/17019/aid/665

3. E. Fleming et al. Is your CMO’s role evolving fast enough? McKinsey & Company, 2015. https://www.mckinsey.com/industries/healthcare-systems-and-services/our-insights/is-your-cmos-role-evolving-fast-enough

4. P. Morgon. Medical Affairs: From Info Gatekeeper to Legitimate Value Driver. Pharmaceutical Executive, 2014. http://www.pharmexec.com/medical-affairs-info-gatekeeper-legitimate-value-driver

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