Senior Clinical Data Analyst

at  IQVIA

EDUCATIONAL REQUIREMENTS:

• BSc/MSc/PhD in Life Science or equivalent work experience in directly related fields (preferably medicine, pharmacy, biotechnology, nursing, or dentistry).

EXPERIENCE:

• 3+ years of experience in Pharmacovigilance, working on clinical studies and/or study safety methodology.
• Good knowledge of ICH/GCP Guidelines.
• Good Knowledge of SAE reporting requirements.
• Computer proficiency with some programming/data science experience (essential: MS Excel, PowerPoint; asset: PowerBI, R-programming, Python).
• Strong attention to detail, analytical skills, and the ability to concisely summarize large amounts of complex information.
• Ability to multi-task in a high-volume environment with shifting priorities.
• Excellent time management skills.
  Team player with the ability to work independently
  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.co

• Collaborate closely with the team to review critical and pre-specified medical (primarily safety) data in clinical trials.
• Generate and manage documents following applicable procedures and best practices, and configure relevant tools.
• Continuously review patient-level clinical/safety data to ensure medical accuracy, completeness, and coding consistency.
• Generate queries as needed for appropriate medical assessment and case closure.
• Schedule and facilitate various types of meetings.
• Create visualizations using relevant tools and prepare slides, reports, and data as required.
• Contribute to non-drug project work, including continuous improvement and development of procedures as needed.
• Update study statuses in the tracker for studies per Therapeutic area upon request.