Mary Coyle
@marycoyle
Experienced product owner and data scientist with a focus on AI.
What I'm looking for
I am an experienced product owner, lecturer, and data scientist with over 10 years of expertise in data analytics, cybersecurity, and pharmaceutical operations. My journey has been marked by a proven ability to lead cross-functional teams, design curricula, and manage product development cycles effectively. I hold a PhD in Artificial Intelligence and am passionate about leveraging data to drive impactful decision-making.
In my recent role as a Senior Data Scientist at Altada, I deployed machine learning models that significantly influenced health, regulatory, and financial decisions. I designed data pipelines using Python, R, and SQL, enabling real-time analytics and reporting. My commitment to mentoring junior analysts and leading internal training reflects my dedication to fostering a collaborative learning environment.
Previously, as a Research Support Manager at PGI, I built AI solutions that addressed complex business challenges in healthcare and finance. My experience managing regulatory compliance for medical device trials at Mias Pharma further solidified my expertise in navigating complex regulatory landscapes. I am eager to continue my professional journey in a role that allows me to innovate and contribute to meaningful projects.
Experience
Work history, roles, and key accomplishments
Senior Data Scientist
Altada
Jan 2020 - Present (5 years 4 months)
Deployed and implemented machine learning models to drive health, regulatory, and financial decision-making. Designed and ran data pipelines using Python, R, and SQL to enable real-time analytics and reporting.
Research Support Manager
PGI
Jan 2018 - Present (7 years 4 months)
Built and implemented deep learning, machine learning, and natural language processing-based AI solutions to solve business problems. Developed end-to-end AI models, from data preprocessing to deployment using TensorFlow, PyTorch, and Scikit-learn.
Compliance Manager for Medical device trials
Mias Pharma
Mar 2014 - Present (11 years 2 months)
Managed regulatory compliance for medical device clinical trials, ensuring adherence to EU MDR, FDA 21 CFR Part 820, and ISO 14155. Coordinated interactions with clinical, regulatory, and quality teams to secure timely submissions and conducted internal audits.
Education
Degrees, certifications, and relevant coursework
Trinity College Dublin
PhD, Artificial Intelligence
Completed a PhD in Artificial Intelligence, focusing on advanced research and development within the field. Gained expertise in complex AI methodologies and applications.
National College of Ireland
MSc, Cybersecurity
Obtained a Master of Science degree in Cybersecurity. Developed a strong understanding of cybersecurity principles, threats, and defense mechanisms.
Munster Technological University
MBS, Investment Funds
Earned a Master of Business Studies in Investment Funds. Acquired specialized knowledge in investment strategies, fund management, and financial markets.
Data Science Institute
MSc, Data Analytics
Completed a Master of Science degree in Data Analytics. Focused on advanced data analysis techniques, statistical modeling, and data-driven decision making.
Griffith College
BA, Pharmaceutical Operations
Completed a Bachelor of Arts in Pharmaceutical Operations. Studied the operational aspects and processes within the pharmaceutical industry.
CCT College Dublin
HDip, Artificial Intelligence
Received a Higher Diploma in Artificial Intelligence. Gained foundational and advanced knowledge in AI concepts and practical applications.
South East Technological University
MSc, Medical Device Technology (Regulatory Affairs)
Attained a Master of Science degree in Medical Device Technology with a focus on Regulatory Affairs. Developed expertise in the regulatory landscape for medical devices.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Job categories
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