Estudiante en Práctica - Regulatory Affairs

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Suba, Bogotá D.C., Distrito Capital
Hybrid
Internship
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
This internship involves assisting with regulatory affairs by managing site activities, supporting data analysis, preparing necessary documentation, and communicating with stakeholders.
Summary Generated by Built In

Why Patients Need You
A career with us is about discovering breakthroughs that change patients' lives. Whatever your role, you'll be part of bringing those therapies to people all over the world. You'll be driving the industry forward and making a positive difference. And you'll discover that amazing things are possible.
What You Will Achieve
In this Co-op/internship/temporary (select one) position, you will have the opportunity to be immersed in an assignment in which you will gain industry experience and help solve some of the biggest challenges we face today. With guidance from your mentor, you will understand the expectations of an employee in a professional setting and how to work independently, as well as within a team, to achieve your project goals. You will be part of a collaborative environment that values diverse thinking and encourages calculated risk taking.
The duration of a co-op assignment is typically 1 year and is almost always paid or has some type of academic credit. This is intended to be an alternative to a full-time classroom study by engaging in discipline-related employment where the work is considered productive to the employer and student.
How You Will Achieve It

  • Manage own time for achieving targets and be accountable for own results.
  • Assist the Site Leads on site management activities and initiatives to ensure effectiveness of the clinical trial safeguarding and data oversight.
  • Assist with analysis that forms the basis of brand strategy, interfacing with
  • cross-functional partners and reporting on findings, and taking the lead on one or
    more strategic or tactical project(s) from start to finish.
  • Keep in touch, under supervision, with national and international Supply Hubs and Headquarter in order to obtain and provide the required support.
  • Help prepare the documents and reports required in the registration and query response dossiers according to the legislation in force.
  • Support the local Pfizer interaction with different stakeholders through the development of materials and participation on initiatives.
  • Maintain, verify, process, and makes updates to systems, spreadsheets or documents.
  • Support the category's market information needs, such as market shares, size of the market and key competitors relying on syndicated data sources.
  • Provide support, information and advice on medical and scientific issues to internal, and external customers.


Qualifications
Must-Have

  • Active enrollment and completion of the 1st year in an accredited, 4 year undergraduate program
  • Knowledge about how to handle national and international databases and other bibliographical sources
  • Highly collaborative and strong communicator
  • Fluent in English


Nice-to-Have

  • Experience working in an office setting


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.
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Top Skills

Bibliographical Sources
National And International Databases

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

Typical time on-site: Not Specified
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