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Regulatory Intelligence Intern Summer 2024 (Remote)

IQVIA is hiring a Regulatory Intelligence Intern for the Summer of 2024. Candidates must be currently pursuing a Masters degree and be available to work East Coast hours.

 

The Regulatory Intelligence Intern will play a crucial role in gathering and managing regulatory information related to drug, biologics, and device approvals. This position involves collating data from various public regulatory sources and collecting internal intelligence within the company.

 

Duties/Responsibilities:

Data Management:

  • Manage, catalog, and review regulatory information obtained from selected regulatory data sources.
  • Ensure accuracy, completeness, and relevance of collected data.
  • Collaborate with cross-functional teams to validate and update regulatory content.

Cataloguing and Documentation:

  • Create and maintain a comprehensive catalog of regulatory products and relevant dimensions of interest.
  • Identify key sources of regulatory information and maintain an organized repository.
  • Document processes for data collection, validation, and storage.

Tool Testing and Optimization:

  • Test the functionality of the regulatory intelligence tool.
  • Identify any issues or discrepancies and collaborate with technical teams to address them.
  • Ensure that the tool operates as designed and meets user requirements.

Process Documentation:

  • Develop clear and concise work instructions for utilizing the regulatory intelligence tool.
  • Create collateral materials (e.g., user guides, FAQs) to support users in navigating the tool effectively.
  • Train relevant stakeholders on using the tool and interpreting regulatory data.

Internal Collaboration:

  • Collaborate with colleagues across departments to gather additional internal intelligence.
  • Assist in analyzing regulatory trends, competitive landscapes, and potential risks.
  • Participate in discussions and contribute insights during internal meetings.

 

Qualifications
• Must be currently pursuing a Masters degree in regulatory science, regulatory affairs, public health, or related life-science field
• Appropriate verbal and written communication skills to function within a professional work environment.
• Evidence of effective problem – solving, analytical, and critical thinking skills.
• Must be able to work East Coast time zone hours
• Evidence of strong team work and communication skills.

 

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

 

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

 

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

 

 

The potential base pay range for this role, when annualized, is $32,200.00 - $48,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.