What are the responsibilities and job description for the Medical Review Specialist position at Abbott?
Job Overview
As a Medical Reviewer/Safety Reviewer at Abbott, you will play a vital role in ensuring the safety and efficacy of our pharmaceutical products. Your expertise will be essential in identifying, evaluating, and resolving significant medical and safety-related issues.
In this role, you will serve as an internal subject matter expert on pharmacovigilance, demonstrating a high level of scientific or technical expertise and an in-depth understanding of drug safety-related processes. You will participate in and oversee compliance of adverse events received for AN products in a compliant and timely manner.
Key Responsibilities:
As a Medical Reviewer/Safety Reviewer at Abbott, you will play a vital role in ensuring the safety and efficacy of our pharmaceutical products. Your expertise will be essential in identifying, evaluating, and resolving significant medical and safety-related issues.
In this role, you will serve as an internal subject matter expert on pharmacovigilance, demonstrating a high level of scientific or technical expertise and an in-depth understanding of drug safety-related processes. You will participate in and oversee compliance of adverse events received for AN products in a compliant and timely manner.
Key Responsibilities:
- Serves as an internal subject matter expert on pharmacovigilance by demonstrating a high level of scientific or technical expertise and an in-depth understanding of drug safety-related processes.
- Participates in and oversees compliance of adverse events received for AN products in a compliant and timely manner.
- Ensures that any reports associated with products registered as pharmaceuticals or with other regulatory requirements for reporting are handled, processed, and submitted according to applicable regulations.
- Maintains documentation and performs quality control checks.
- Reviews literature search results and handles processing and maintenance of safety-related data found in literature.
- Reviews aggregate safety data for inclusion in periodic reports, signal reports, and other pharmacovigilance-related documents.
- Assists in maintaining global processes and procedures that are aligned with good pharmacovigilance practices.
