Clinical Information Science Associate Director, Cardiovascular, Renal and Metabolism

AstraZeneca • Gaithersburg, MD

1d

About The Position

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. Most importantly, we do meaningful work that changes lives. It’s our purpose that drives us, every day. Would you like to play an essential role in helping patients who need it the most?
If yes, explore the possibility of joining us as a Clinical Information Science Associate Director, within Cardiovascular, Renal and Metabolism (CVRM). The position sits within our Information Practice unit, a part of the Late-stage CVRM Biometrics organisation. Late-stage CVRM Biometrics consists of statistics, programming, data science and information experts for drug development in phase II and beyond. You will be part of a truly global team alongside some of the most respected specialists in the industry.
What you’ll do
As a strategic information expert embedded within dynamic drug project teams, you will lead the delivery of information that clinical teams need to make decisions in the drug development process. You will be an authority on innovative use of information and data to help shape our trials and portfolio.
You will use a variety of information sources such as scientific literature, competitive intelligence, internal and external clinical trial databases and techniques such as specialist information search and analysis, data visualization and benchmarking to extract and present key relevant information.
You will be accountable for Information Practice delivery scope in one or more drug projects by own contribution or leadership of other information practice staff, partners and suppliers. You will lead or contribute to proactive development and execution of the Project Information Strategy, providing foresight into what information will be needed to support upcoming drug project needs to achieve goals and milestones, and to drive the active re-use of Information assets and clinical data.

Requirements

• Master’s degree in Life Science, Computer Science, Information Science or equivalent experience
• Significant experience in the application of information and knowledge management in a clinical or scientific setting (settings could include, but are not limited to clinical drug development, medical writing, medical affairs, clinical operations, competitor intelligence, regulatory intelligence)
• Understanding of the pharmaceutical clinical drug development process (with a preference for late-stage drug development in cardiovascular, renal, and metabolism)
• Excellent communication skills, including proficiency in communicating complex information to a diverse audience
• Demonstrated leadership capability, including ability to influence stakeholders
• Good organizational skills and the ability to set priorities and follow a timeline
• Great attention to detail

Responsibilities

• Support decision-making in clinical design, submission and interpretation by identifying, extracting and presenting back meaningful facts and data via internal and external information sources
• Enable quality decisions by providing comprehensive access to key decisions and rationale for study designs and project milestones from phase II and throughout the project life cycle, helping the organization to grow and maintain scientific knowledge
• Information strategy for project and TA, proactively assessing information gaps that needs to be filled, enable re-use of information between project and TA and define new ways of working cross projects applying knowledge of external environment and trends
• Organize and structure information for drug development decisions and for reuse of information and data

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level