Send us a text

Marie Pihl’s journey from an assistant nurse with dreams of working in a children's hospital to becoming the Director of Operations, Technology, and Analytics in Global Patient Safety at AstraZeneca is nothing short of inspiring. Her story is one of perseverance, adaptability, and the power of commitment, as she balanced further education in molecular biology while raising three children. Marie's 21-year career at AstraZeneca, marked by pivotal experiences like training a vendor team in Budapest, showcases the transformative potential of embracing challenges and seizing opportunities.

Join us as we explore the shifting dynamics of career development in the pharmaceutical industry. With traditional linear career paths being reimagined, the importance of gaining broad experience and embracing lateral moves is more crucial than ever. We'll discuss how fostering a collaborative and open team environment can lead to immense growth and innovation, and the role social media plays in shaping career expectations. This episode also delves into the need for cross-functional understanding at organizations like AstraZeneca to ensure cohesive progress across various expert areas.

Finally, we uncover AstraZeneca’s strategic approach to vendor collaboration and oversight, emphasizing the balance between strategic control and operational efficiency. Through the analogy of a garden, we explore the continuous care required in pharmacovigilance and the cautious optimism surrounding the integration of automation and AI. Listen in for insights on maintaining adaptability, learning from setbacks, and the critical role human oversight plays in technological advancements, as we ponder the future landscape of pharmacovigilance.

Send us a text

What can we learn from a leader at the forefront of pharmacovigilance and risk management? Thomas Kuckuk, Head of System Operations Management at Novartis, offers an insightful journey through his career, weaving through medical informatics and into the heart of the pharmaceutical industry. This episode promises to illuminate the dynamics of safety technology and strategic program implementation, highlighting the critical differences between development and commercial settings that have shaped his professional path.

We delve into the world of AI, exploring its revolutionary role in safety technology and distinguishing between genuine AI applications and basic automation. The conversation sheds light on the pressing challenges of scaling AI solutions within large corporations and the fragmented software vendor landscape. Insights from the World Drug Safety Congress underscore the urgent need for innovation, steering away from the redundant reinvention of existing solutions, and pushing for a unified approach that truly adds business value.

Thomas and I also tackle the potential of industry-wide collaboration, especially in the context of cloud-based vendor landscapes. We discuss the impact of vendor lock-in on innovation and the promising avenues of adopting standardized data models to foster a competitive environment. By encouraging collaboration and balancing market forces, we aim to enhance patient safety and efficiency, unlocking new possibilities for both large and small players in the pharmaceutical world. Join us for a thought-provoking session that explores the potential of driving innovation through strategic industry partnerships.

Send us a text

Sabura Matthews, a visionary in digital strategy for global patient safety, shares her transformative journey from the fast-paced world of trauma nursing to the strategic realm of pharmacovigilance. Her story begins amidst the chaotic energy of Philadelphia's trauma centers, where she honed her critical care skills. Facing professional challenges and yearning for growth, Sabura transitioned into clinical data management at SmithKline Beecham, where she discovered the powerful intersection of technology and patient safety. Her evolution serves as an inspiring blueprint for those looking to pivot their careers while leveraging their unique expertise.

Listeners will gain insights into the dynamic nature of pharmacovigilance careers as we dissect the shifting landscape over the years. The rise of AI and the prevalence of vendor outsourcing have redefined opportunities, particularly in roles focused on case processing. Sabura shares valuable strategies for career development, emphasizing the importance of proactive learning. From attending industry events to consuming educational content, she highlights the need to continuously expand one's skill set. This episode promises actionable advice for anyone eager to navigate and succeed in an ever-evolving industry.

We also explore the complexities of project management and the critical role of digital tools in enhancing operational efficiency. The conversation dives into the nuances of balancing outsourcing with maintaining control over essential processes, stressing the danger of excessive dependence on vendors. Sabura's insights offer a guide to optimizing internal operations and ensuring compliance with the latest regulatory and technological standards. Listen to this enriching dialogue for thoughtful perspectives on aligning digital solutions with business needs, fostering strong vendor relationships, and ultimately achieving successful project outcomes.

Send us a text

What do you get when you combine a background in neurobiology with a serendipitous introduction to pharmacovigilance? Join us as Sibel Guerler, Head of Strategy and Safety Evaluation at BMS, takes us on her remarkable journey, where life's unexpected turns have led to a fulfilling career in drug safety. Transitioning from managing databases and hard copies to embracing cutting-edge technologies, Sibel’s story is a testament to adaptability and the power of seizing opportunities. Her insights offer a compelling look at how passion and a supportive environment can transform a career into a calling.

Explore the highs and lows of working within large organizations like J&J, as Sibel recounts her early days of navigating complex structures and learning from seasoned mentors. From establishing an oversight group to managing diverse responsibilities in smaller markets, her experiences illuminate the intricate world of pharmacovigilance and the importance of cultivating leadership skills. The episode unfolds with her transition to Celgene, where her enthusiasm for technological innovation reshaped her professional path, showcasing the dynamic evolution of roles in safety management.

As Sibel reflects on the broader shifts in pharmacovigilance over the last two decades, we uncover the impact of pivotal FDA and EMA legislations and the pressing need for modern, agile approaches to safety. With a focus on integrating safety considerations into digital health ideation, she challenges outdated frameworks and highlights the strategic role of safety teams in the competitive landscape of drug development.

Send us a text

Ever wondered how a liberal arts major, MBA holder, and former infantry officer navigates the complex world of pharmacovigilance? Our special guest, Richard Wolff, Vice President of Client Relations at RxLogix, shares his unique journey and insights. Richard's diverse background and rich experience at Johnson & Johnson tackling global adverse event reporting reveal the meticulous precision and regulatory understanding required in the field. Listen as Richard reflects on how fresh perspectives can challenge established processes to enhance efficiency and maintain patient safety.

Transitioning into mid-sized companies, Richard discusses the strategic roadmap essential for growth in PV, drawing from his experiences at CSL. He delves into the intricacies of building capabilities, managing inspection observations, and implementing new safety systems while maintaining workforce stability. Hear about his exciting new role at RxLogix and the pressing challenges in the PV industry, including the impact of AI and the complexities of modern PV departments. Discover how regulatory inspections can serve as opportunities for organizational reset amidst increasing complexities.

Pharmacovigilance is not without its challenges, and Richard provides an in-depth look at cost pressures, regulatory changes, and the adoption of advanced technologies like AI and RPA. He explores the implications of these innovations on long-term costs and risks, highlighting the necessity of structural innovation to propel the field forward. Uncover the importance of balancing technology with human expertise to ensure patient safety, and how vendors, service providers, and pharma companies must organize effectively to meet rising expectations. Tune in for a riveting conversation on the evolving landscape of pharmacovigilance and the critical role of structural changes in its future.

Send us a text

Embark on a captivating journey with Nicole Baker, the pioneering CEO of Biologit, as she shares her remarkable transition from academia to the forefront of pharmacovigilance on Truliant Talks. Nicole's narrative is not just about her personal evolution but also serves as an illuminating guide through the labyrinth of safety regulations and drug monitoring. Her candid conversation is a deep dive into the importance of patient safety, the impact of regulatory shifts, and the ever-present need for industry adaptability. We examine the significance of professional networks and the influence of major events like Brexit, providing an insightful look at how these factors have reshaped the European pharmacovigilance landscape.

As technology becomes increasingly intertwined with pharmacovigilance, Nicole lays out her experiences in harnessing AI to revolutionize the field. She reflects on the challenges of setting up a department during Brexit and the subsequent founding of a consultancy aimed at developing accessible AI models for the industry. We unravel the intricacies behind AI and automation, discussing their roles in improving the efficiency and accuracy of adverse event detection. The synergy between pharmacovigilance professionals and technology is spotlighted, as we explore the cautious optimism surrounding AI's potential and the journey from skepticism to acceptance within the industry.

Finally, we turn our attention to the future, speculating on how integration within pharmacovigilance could transform safety data analysis and application. We discuss the necessity of a broader perspective in adverse event reporting, touching upon the current inefficiencies and the potential for systems that ensure data accuracy and consistency. With Nicole's valuable insights, we conclude with aspirations for these advancements to materialize over the next five years, revolutionizing how we understand and manage drug safety. Tune into Truliant Talks for an episode that promises to broaden your horizons on the pivotal role of pharmacovigilance in healthcare.

Send us a text

Embark on a transformational trek with Bill Ringbloom, AstraZeneca's Head of Global Patient Safety Technical Solutions as he shares his unconventional career trajectory from the financial chaos of 2008 to the cutting edge of pharmacovigilance. With a treasure trove of experience spanning IT, finance, and project management, Bill's insights shed light on the value of adaptable skill sets in the ever-evolving pharmaceutical domain. Tune in and uncover how the fusion of these diverse abilities is not just enhancing global patient safety but is also shaping the strategic role of IT within the healthcare juggernaut.

In the heart of our exchange, Bill dissects the intricate dance between finance and life sciences, proving that the two are more intertwined than one might assume. The conversation reveals how the flexibility of IT not only supported AstraZeneca through the pandemic but also bolstered the rollout of their vaccine. Listen closely as we navigate the thought-provoking parallels that bridge two seemingly disparate worlds, reinforcing the significance of financial prowess in steering the ship of innovation amidst a sea of stringent industry demands.

The episode culminates with a deep dive into the frontiers of data strategy and the monumental efforts in cloud migration for drug safety. Bill elucidates the vision for a 'data supermarket'—where data is not just abundant but actionable—and the intricate balance necessary when enhancing surveillance to serve scientific use cases. Grasp the complexities of IT decisions that are transforming patient safety and R&D processes as we explore how AstraZeneca is steering towards predictive analytics in pharmacovigilance, all while navigating the need for efficiency and the pursuit of scientific precision.

Send us a text

Embark on an enlightening expedition, as we navigate the vital intricacies of pharmacovigilance and risk management alongside Tom Nichols, zoologist turned PV aficionado and Director of Drive Phase PV. Tom regales us with his unexpected but inspiring foray into the world of drug safety, stemming from a keen interest in epidemiology. His captivating tales underscore the importance of PV in delivering life-saving therapies to market, particularly through his work with Clozapine, an anti-psychotic medication. This conversation is a testament to PV's dual role as both a guardian of public health and a strategic ally in expediting breakthrough medical treatments.

Tom then delves into the nuances of integrated clinical trial sponsorship and how this model encourages collaboration across the pharmaceutical landscape. Reflecting on my own career trajectory, he offer's a candid comparison of working within the close-knit fabric of clinical research versus the challenges posed by outsourcing, providing a glimpse into the dynamic nature of our industry.

As the journey concludes, Tom explores the landscape of future pharmacovigilance strategies, where the deployment of AI could revolutionize patient safety protocols, and the delicate balance between swift drug access and thorough post-market analysis is ever-present. Tom's insights, coupled with moments of passionate discourse, have been nothing short of invigorating. Join us for a conversation that promises not only to inform but to inspire a deeper appreciation of pharmacovigilance.

Send us a text

Discover the intricate world of pharmacovigilance as Colleen Walsh, the Vice President of Global Patient Safety Operations at Alnylam, unveils her personal journey through the ever-evolving landscape of patient safety. In this enthralling episode of Innovation and the Future of Pharmacovigilance, I sit down with Colleen to unravel the complexities she's encountered, from the pivotal Tysabri incident at BioGen to leading R&D compliance at Alexion. Her story is a testament to the resilience required in the face of regulatory upheavals and the innovative spirit needed to navigate from clinical trials to post-market safety.

In a field where the stakes are as high as the patients' lives, Colleen sheds light on the arduous task of merging companies within the rare disease sector, specifically the AstraZeneca acquisition of Alexion. Through her insights, we gain an understanding of the delicate balance between patient support programs and the scrutiny of global pharmacovigilance regulations. Colleen's expertise reveals the pressing need to bridge the gap between regulatory intent and its real-world application, ensuring that patient safety remains paramount while fostering a culture of innovation.

Our discussion veers into the future of pharmacovigilance technology, examining how AI could revolutionize the industry yet poses unique challenges for both behemoths and fledgling companies in the pharmaceutical world. Colleen proposes an intriguing shift in perspective, advocating for pharmacovigilance to transition from a cost burden to a revenue generator by incorporating safety measures early in drug development. Join us on this episode as we probe into a future where pharmacovigilance not only safeguards patients but also drives value and progress in the realm of medicine.

Send us a text

Embark on an insightful exploration of pharmacovigilance with me, Indy Ahluwalia, as I sit down with industry trailblazer Rishi Chopra on Truliant Talks. Witness the fascinating narrative of Rishi's transition from biochemistry academia to becoming an instrumental figure in the pharmacovigilance space. His candid recount of the early days at Roche, where a nurturing community played a crucial role in his growth, sets the stage for a discussion full of personal anecdotes and pivotal moments that define a career. We delve into the essence of mentorship and the power of connections that transcend roles, highlighting Rishi's journey from his initial foray into the field to his current influential position.

Prepare to be inspired as Rishi unfolds the map of his leadership voyage, from establishing compliance frameworks to lecturing at universities, blending academic rigor with invaluable industry experience. His tales from the trenches at Otsuka, Biogen, and now CSL showcase the continuous learning and the unyielding pursuit of patient safety under the mentorship of industry luminaries. The chapter not only sheds light on overcoming challenges and celebrating triumphs but also on the diverse cultural insights gained from working with global teams.

As the healthcare landscape evolves, so do the tools and technologies shaping its future. Rishi lends his global perspective on the burgeoning role of artificial intelligence and the potential of social media in revolutionizing patient data collection. The conversation turns to the frontiers of personalized medicine and the anticipation of new roles that will merge technology with patient care. Our episode culminates with an eye on harmonizing global regulations, ensuring that, through collaboration and innovation, patient safety remains at the heart of pharmacovigilance. Join us for a riveting dialogue that promises to leave you enlightened and excited about the future of healthcare.