Safety Data Management Specialist
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Job Location:
Parsippany, NJ - USA
Monthly Salary:
$ 71800 - 119600
Posted on:
25-10-2025
Vacancies:
1 Vacancy
Job Summary
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 Pfizers customers and patients to receive the medicines they need when they need them.
How You Will Achieve It
- Carry out case processing activities.
- Review rank verify process and document case-related information: event terms; validity seriousness special scenarios; timelines; accuracy and consistency. Process cases based on these assessments.
- 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
Qualifications
Must-Have
Bachelors Degree in Health or Life Sciences
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
Demonstrated computer literacy
Fluency in spoken and written English
Nice-to-Have
Health Care Professional or equivalent experience preferred.
1 years experience in pharmacovigilance and/or data management preferred but not required
Experience and skill with medical writing an advantage
Experience in use and management of relational databases preferred
Other job details:
Last date to Apply for Job:
Work Location Assignment:This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & 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 disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing please email. This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and/or interviewing. Requests for any other reason will not be returned.
Required Experience:
IC
Key Skills
- Microsoft Office
- Computer Skills
- Construction Experience
- Food Safety Experience
- Root cause Analysis
- Microsoft Powerpoint
- OSHA
- Child Protective Services
- EPA
- Unity
- EHS
- Manufacturing
About Company
Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.
