What are the responsibilities and job description for the Global Adverse Event Reporting Expert position at Pharma Search Partners LLC?
Responsibilities
The successful candidate will be responsible for evaluating the need for follow-up on adverse event reports that may impact the safety profile of product areas. They will implement a quality control process to verify the accuracy, completeness, and validity of information for adverse event reports.
This role involves interaction with health professionals and consumers regarding post-market adverse experiences, as well as assistance in projects requiring review and assessment of medical information obtained or related to adverse event reports.
Key Responsibilities
- Quality control process implementation
- Follow-up on adverse event reports
- Collaboration with cross-functional teams
Requirements
- Knowledge of International and US Regulations for reporting Adverse Events
- Minimum 5-7 years of experience in an industry application of clinical medicine/pharmacy
