Fresher Needed Safety Surveillance Associate at Pfizer
Pfizer, a global leader in pharmaceuticals, is looking for Safety Surveillance Associates to join its team in Chennai. This role offers an exciting opportunity for freshers to experienced professionals (0-6 years) who are passionate about contributing to global healthcare by ensuring the safety and compliance of Pfizer’s extensive product portfolio.
Key Job Highlights
- Position: Safety Surveillance Associate
- Experience: 0-6 Years (Freshers Welcome)
- Location: Chennai, India
- Skills: Pharmacovigilance, Medical Writing, Communication, Database Management
- Responsibilities: Case processing, safety report generation, collaboration with clinical teams.
- Qualifications: Degree in Pharmacy, Dentistry, Nursing, or related field.
Why Join Pfizer as a Safety Surveillance Associate?
Pfizer is known for its innovative medicines and vaccines that improve the lives of people across the globe. As a Safety Surveillance Associate, you’ll be an essential part of the company’s commitment to patient safety. This role focuses on ensuring that Pfizer’s products meet stringent safety standards during both clinical trials and post-marketing phases. If you’re passionate about pharmacovigilance, compliance, and playing a key role in maintaining public health, this job is for you.
Primary Responsibilities
Case Processing and Prioritization
In this role, you will be responsible for identifying and selecting cases for processing. You’ll prioritize cases based on urgency and document any reasons for delays. This requires a sharp eye for detail and the ability to make quick, informed decisions.
For more complex cases, you will be tasked with assessing and escalating them to the appropriate teams. This ensures that critical safety data is handled by the right experts, contributing to Pfizer’s overall goal of maintaining the highest safety standards for its product portfolio.
Event Review and Reportability
You’ll also engage in the review and classification of event terms, as well as managing product complaint information. Ensuring that reports are accurate and comply with regulatory standards is crucial, as safety surveillance plays a key role in both clinical and post-marketing settings.
Your work will include writing and editing case narratives, ensuring that these adhere to regulatory compliance timelines. This task is critical, as case narratives form the backbone of pharmacovigilance documentation, providing clear, concise summaries of each safety event.
Safety Reports and Collaboration
One of your key responsibilities will be to generate safety reports and determine if any follow-ups are necessary. These reports are vital in helping regulatory bodies, healthcare providers, and Pfizer’s internal teams understand the safety profile of the company’s products.
Additionally, you’ll work closely with Pfizer’s Country Organizations, Clinical Development teams, and License Partners. Collaboration ensures that data is properly collected, reconciled, and used to make informed decisions regarding product safety.
Expertise Development
As you progress in this role, you will develop deep expertise on Pfizer’s product portfolio, understanding both its clinical applications and safety risks. You will also gain knowledge of corporate regulations, global guidelines, and Standard Operating Procedures (SOPs), which will guide your daily work.
Pfizer places a high emphasis on adhering to regulatory requirements, so it is essential that you consistently apply these standards and policies across all your tasks. This not only helps protect patients but also maintains Pfizer’s reputation as a global leader in healthcare.
Technical Skill Requirements
To succeed as a Safety Surveillance Associate, you should have experience or the ability to quickly learn pharmacovigilance processes. Experience in clinical care or clinical/scientific research is highly advantageous. You will need to be proficient in relational databases, as data management is a crucial part of the job.
Good oral and written communication skills are essential. You’ll be writing detailed case narratives, so strong proficiency in English is required. If you know any additional languages, that’s a bonus, as Pfizer operates globally, and being multilingual can be a valuable asset.
Experience in medical writing is also a plus, as you will often need to communicate complex medical and scientific information in a clear, precise way.
Qualifications
To apply for this role, candidates should have a degree in a healthcare-related field, such as Pharmacy, Dentistry, or Nursing. Pfizer welcomes applicants with 0 to 6 years of relevant experience in pharmacovigilance, clinical research, or related fields.
The ability to work under supervision and collaborate in a matrix organization is crucial, as Pfizer encourages teamwork and cross-functional collaboration.
Application Link
Conclusion
Joining Pfizer as a Safety Surveillance Associate offers a unique opportunity to be at the forefront of ensuring patient safety in both clinical trials and the global market. Whether you’re a fresher or have up to 6 years of experience, this role will allow you to make a meaningful impact while advancing your career in a world-class pharmaceutical company. If you’re passionate about healthcare and safety, this is your chance to contribute to life-saving work at a global scale.