Safety Data Management Specialist
Pfizer
Date: 9 hours ago
City: Makati City
Contract type: Full time
Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will Achieve
You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them.
How You Will Achieve It
Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
Review case criteria to determine the appropriate workflow for case processing.
Position Purpose
Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports.
Primary Responsibilities
Review case criteria to determine appropriate workflow for case processing.
Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.
Write and edit case narrative.
Determine and perform appropriate case follow-up, including generation of follow-up requests.
Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.
Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.
Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.
Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.
Consistently apply regulatory requirements and Pfizer policies
Participate, as appropriate, in local, internal, and external safety activities
Technical Skill Requirements
Demonstrated computer literacy.
Qualifications
Experience in use and management of relational databases preferred
Health Care Professional Or Equivalent Experience Preferred.
Ability, with supervision, to solve routine problems and to surface issues constructively.
Ability to make basic decisions with an understanding of the consequences.
Ability to achieve personal objectives while meeting departmental standards of performance.
Ability to work under supervision in a matrix organization.
Fluency in spoken and written English
Physical/Mental Requirements
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will Achieve
You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them.
How You Will Achieve It
- Contribute to completion of project milestones and organize own work to meet project task deadlines.
Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
Review case criteria to determine the appropriate workflow for case processing.
Position Purpose
Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports.
Primary Responsibilities
- Carry out case processing activities.
Review case criteria to determine appropriate workflow for case processing.
Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.
Write and edit case narrative.
Determine and perform appropriate case follow-up, including generation of follow-up requests.
Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.
Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.
Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.
Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.
Consistently apply regulatory requirements and Pfizer policies
Participate, as appropriate, in local, internal, and external safety activities
Technical Skill Requirements
- Experience in pharmacovigilance and/or data management preferred
Demonstrated computer literacy.
Qualifications
Experience in use and management of relational databases preferred
- 1+ years of pharmacovigilance experience preferred
Health Care Professional Or Equivalent Experience Preferred.
Ability, with supervision, to solve routine problems and to surface issues constructively.
Ability to make basic decisions with an understanding of the consequences.
Ability to achieve personal objectives while meeting departmental standards of performance.
Ability to work under supervision in a matrix organization.
Fluency in spoken and written English
Physical/Mental Requirements
- Must have the “ability to communicate,” “ability to work on teams”, “office job involving use of computer”, etc.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
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