Clinical Trial Hub Safety Associate

Posted 2 Days Ago
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San Jose, Escazu, Escazu
Junior
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
As a Clinical Trial Hub Safety Associate, you will oversee the company's drug safety program, manage adverse reports, ensure compliance with regulations, prepare safety-related reports, and mentor colleagues while maintaining knowledge of pharmaceutical products.
Summary Generated by Built In

Use Your Power for Purpose
Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.
What You Will Achieve
In this role, you will:

  • Monitor and manage the company's drug, biologics, and medical devices surveillance program, ensuring comprehensive oversight.
  • Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities, ensuring accurate and timely handling.
  • Act as a subject matter expert, liaising with key partners regarding safety data collection, reconciliation, and ensuring regulatory compliance.
  • Review, analyze, prepare, and complete safety-related reports to determine the safety profile of products and meet regulatory requirements.
  • Verify the accuracy, consistency, and compliance of processed cases, and review case data for special scenarios, ensuring high standards are maintained.
  • Manage safety resources within the local team, provide specific pharmacovigilance or product knowledge, mentor colleagues, and maintain advanced knowledge of Pfizer's product portfolio and corporate policies.


Here Is What You Need (Minimum Requirements)

  • BA/BS with at least 2 years of experience or MBA/MS with any years of experience
  • Strong organizational and project management skills
  • Solid knowledge of global regulations and guidelines for drug development
  • Demonstrated analytical and statistical skills
  • Fluency in spoken and written English


Bonus Points If You Have (Preferred Requirements)

  • Master's degree
  • Relevant pharmaceutical industry experience
  • Familiarity with management of performance metrics
  • Strong problem-solving skills
  • Proficiency in safety database and data mart search functions


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.
Medical
#LI-PFE

Top Skills

Adverse Reports Evaluation
Drug Surveillance Program
Pharmacovigilance
Regulatory Compliance
Safety Database
Safety-Related Reports

What the Team is Saying

Daniel
Anna
Esteban
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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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