Colleagues from Pfizer Worldwide Medical and Safety are crucial in connecting stakeholders and coworkers with evidence-based medical decision support to improve health and treatment outcomes. Our aim is straightforward, whether you are developing the framework required to make sure our evidence is scientifically sound, offering unbiased, medically essential knowledge, or looking at ways to overcome data gaps. empower people to participate in decisions about the safe and appropriate use of medications.
Position: Associate – Safety Data Management
Qualifications
Must-Have
1. Only B. Pharm qualification.
2. 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.
3. Decent knowledge of pharmacovigilance regulations, solid analytical skills, and very keen attention to detail!
Nice-to-Have
1. Direct experience in the ARGUS safety database and with E2B case processing.
2. Good academic and/or extra-curricular accomplishments.
What You Will Achieve
1. 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.
2. 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.
3. 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
1. Contribute to completion of project milestones and organize own work to meet project task deadlines.
2. Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.
3. Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
4. Review case criteria to determine the appropriate workflow for case processing.
Work Location Assignment: Flexible
 
 
 
