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Clinical Trial Coordinator
2 weeks ago
Pfizer is a global biopharmaceutical company dedicated to delivering innovative therapies that improve lives. As a Safety Data Management Specialist, you will play a crucial role in ensuring the safe and effective use of our products.
Job DescriptionYou will be responsible for monitoring the company's drug surveillance program for adverse events, evaluating and processing adverse reports from clinical trials and post-marketing activities, and providing expertise on regulatory requirements and corporate policies for regulatory submissions.
Key Responsibilities:
- Monitor drug surveillance programs for adverse events.
- Evaluate and process adverse reports from clinical trials and post-marketing activities.
- Provide expertise on regulatory requirements and corporate policies for regulatory submissions.
- Analyze post-marketing safety data and review medical literature to support Worldwide Strategy and Regulatory teams.
Requirements:
- Bachelor's degree in a relevant field with any years of experience.
- Strong analytical skills with the ability to interpret complex data.
- Proficiency in using safety databases and software.
- Excellent written and verbal communication skills.
