Pharmacovigilance Senior Specialist

Metacom Careers; Taguig; On-site; PHP 300,000 - 420,000; Full time

Job summary

Metacom Careers seeks a Pharmacovigilance Associate in the Philippines to monitor and assess adverse drug reactions, conduct safety case processing, and prepare regulatory reports. You will work with cross-functional teams to ensure compliance with safety regulations in a fast-paced environment.

The role requires 2–5 years of pharmacovigilance experience, a Life Sciences degree, and proficiency with Veeva Safety Database and Argus, plus strong analytical skills and meticulous attention to

Qualifications

• Educational Qualifications: Bachelor’s degree in Life Sciences or related field.
• Experience Level: 2–5 years of experience in pharmacovigilance.
• Skills and Competencies: Proficiency in safety case processing, Veeva Safety Database, and Argus.
• Qualities and Traits: Strong analytical skills and attention to detail.
• Responsibilities and Duties: Knowledge of regulatory requirements and guidelines.
• Working Conditions: Comfortable working in a fast-paced, deadline-driven environment.

Responsibilities

• Monitor and assess adverse drug reactions and safety signals.
• Conduct safety case processing and maintain accurate documentation.
• Utilize Veeva Safety Database and Argus for data management and reporting.
• Prepare safety reports and submit to regulatory authorities.
• Collaborate with cross-functional teams to ensure compliance with safety regulations.

Skills

Proficiency in safety case processing

Veeva Safety Database

Argus

Analytical skills

Attention to detail

Education

Bachelor's degree in Life Sciences

Job description

• Monitor and assess adverse drug reactions and safety signals.
• Conduct safety case processing and maintain accurate documentation.
• Utilize Veeva Safety Database and Argus for data management and reporting.
• Prepare safety reports and submit to regulatory authorities.
• Collaborate with cross-functional teams to ensure compliance with safety regulations.

Description

• Monitor and assess adverse drug reactions and safety signals.
• Conduct safety case processing and maintain accurate documentation.
• Utilize Veeva Safety Database and Argus for data management and reporting.
• Prepare safety reports and submit to regulatory authorities.
• Collaborate with cross-functional teams to ensure compliance with safety regulations.

Requirements

• Educational Qualifications: Bachelor's degree in Life Sciences or a related field
• Experience Level: 2-5 years of experience in pharmacovigilance
• Skills and Competencies: Proficiency in safety case processing, Veeva Safety Database, and Argus
• Qualities and Traits: Strong analytical skills and attention to detail
• Responsibilities and Duties: Knowledge of regulatory requirements and guidelines
• Working Conditions: Comfortable working in a fast-paced, deadline-driven environment