Regional Regulatory Science Hub Strategist

Posted Yesterday
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Suba, Bogotá D.C., Distrito Capital
Hybrid
Mid level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The role involves understanding hub procedures, navigating regulatory requirements, and improving submission strategies to support Pfizer's initiatives.
Summary Generated by Built In

Use Your Power for Purpose
Your dedication and expertise are crucial in bringing medicines to the world faster without compromising on excellence and integrity. Adhering to both local and global regulations is essential, especially in an ever-changing regulatory environment that demands forward thinking and meticulous attention to detail. By maintaining these high standards, you will help expand and accelerate patient access to Pfizer medicines and vaccines. Your role is vital in ensuring that we meet these challenges head-on, providing the necessary support to navigate complex regulations and ultimately deliver life-saving treatments to those in need.
What You Will Achieve
In this role, you will:

  • Possess a thorough understanding and application of the Hub procedures.
  • Understand local regulations and trends, as communicated by the CRS.
  • Utilize a submission planning and forecasting tool to update timelines when necessary.
  • Update the appropriate regulatory requirements systems and database promptly when market regulations change.
  • Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values and which supports compliance, innovation and talent development and retention, as needed
  • Complete departmental training in a timely manner to address corporate and regulatory compliance.
  • Drive improved efficiencies across the region through achieving consistency in submission strategies and its execution. Make suggestions and recommendations that contribute to improvements in the Hub.
  • Maintain an active partnership with counterparts across the Hub Regional team


Here Is What You Need (Minimum Requirements)

  • Bachelor's degree or equivalent
  • Experience in regulatory affairs, preferably in human medicines
  • Demonstrated experience and a proven ability to consistently deliver to time, cost, and quality standards
  • Excellent organizational skills and attention to detail
  • Knowledge of documentation practices
  • Fluency in English, both verbal and written


Work Location Assignment: Hybrid
EEO (Equal Employment Opportunity) & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
Regulatory Affairs
#LI-PFE

Top Skills

Databases
Regulatory Requirements Systems
Submission Planning And Forecasting Tool

What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Pfizer Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Typical time on-site: Not Specified
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