Freshers BPharm Associate – Safety Data Management Job at Pfizer
Locations: India – Chennai
Time Type: Full time
Posted On: Posted Today
Job Requisition ID: 4892897
About Pfizer
Pfizer is a global pharmaceutical company committed to improving health and treatment outcomes. Our Worldwide Medical and Safety colleagues play a vital role in connecting evidence-based, medical decision support with colleagues and stakeholders. We empower healthcare decisions regarding the safe and appropriate use of medicines for patients by ensuring scientifically sound evidence, providing unbiased expertise, and closing gaps in data.
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 to 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 your own work to meet project task deadlines.
- Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.
- 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.
Qualifications
Must-Have
- ONLY B. Pharm qualification.
- Direct work experience in Pharmacovigilance, ICSR (Individual Case Safety Reports) processing of NO MORE THAN 2 years. B. Pharm freshers are also welcome to apply.
- Decent knowledge of pharmacovigilance regulations, solid analytical skills, and very keen attention to detail!
Nice-to-Have
- Direct experience in the ARGUS safety database and with E2B case processing.
- Good academic and/or extra-curricular accomplishments.
Work Location Assignment: Flexible
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