Safety Surveillance Associate

Pfizer; Makati; Hybrid; PHP 500,000 - 800,000; Full time

Job summary

A leading pharmaceutical company in Metro Manila seeks a professional for a pharmacovigilance role. You will monitor drug safety and evaluate adverse reports. Candidates should have a BS in Pharmacy or Nursing, strong analytical and communication skills. This role offers a hybrid work environment.

Qualifications

• Strong analytical skills with the ability to interpret complex data.
• Excellent written and verbal communication skills.
• Basic understanding of regulatory requirements and corporate policies.

Responsibilities

• Monitor the company's drug, biologics, and medical devices surveillance program.
• Evaluate and process adverse reports for clinical trials and post-marketing activities.
• Support Worldwide Strategy and Regulatory teams by analyzing safety data.

Skills

Analytical skills

Communication skills

Team collaboration

Education

BS in Pharmacy or Nursing

Tools

Safety databases and software

Job description

**Use Your Power for Purpose**At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.**What You Will Achieve**In this role, you will:* Monitor the company's drug, biologics, and medical devices surveillance program.* Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities.* Make decisions within limited options to resolve problems, under the supervisor's direction.* Work in a structured environment, following established procedures.* Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.* Provide expertise on regulatory requirements and corporate policies for regulatory submissions to project teams.* Support Worldwide Strategy and Regulatory teams by analyzing post-marketing safety data, reviewing medical literature, and related activities.* Determine the appropriate workflow for case processing by reviewing case criteria.**Here Is What You Need** (Minimum Requirements):* BS in Pharmacy or Nursing, passed the board exam* Strong analytical skills with the ability to interpret complex data* Proficiency in using safety databases and software* Excellent written and verbal communication skills* Ability to work collaboratively in a team environment* Basic understanding of regulatory requirements and corporate policies**Bonus Points If You Have** (Preferred Requirements):* Experience in pharmacovigilance or drug safety* Familiarity with medical terminology and coding systems* Knowledge of global regulatory requirements for drug safety* Strong problem-solving skills and the ability to make decisions with limited information* Proficiency in multiple programming languages and frameworks* Experience with cloud platforms and services* Familiarity with agile methodologies and project management toolsWork Location Assignment: Hybrid#LI-PFEPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.MedicalKarrieren bei Pfizer sind einzigartig. In unserer Kultur der individuellen Verantwortung glauben wir an unsere Fähigkeit, die Zukunft der Gesundheitsversorgung zu verbessern und an unser Potenzial, viele Millionen Leben zum Besseren zu wandeln. Wir suchen stets nach neuen Talenten für unsere globale Gemeinschaft, um gemeinsam neue innovative Therapien zu entwickeln, die die Welt zu einem gesünderen Ort machen.