Med Info Spec I
Core
Provides technical and medical information and manages intake of adverse events and product complaints for pharmaceutical or device products.
Role type
Medical Information Specialist
Builds
Clinical trial information and regulatory-compliant responses for clients
Domain
Life Sciences / Pharmaceuticals / Medical Devices
Deliverable
client delivery
Required skills
Medical information analysis, Adverse event triage, Regulatory guideline compliance, Medical literature research, Database documentation, Technical inquiry resolution
Preferred skills
None stated
Technologies
None stated
Responsibilities
Respond to technical and medical inquiries via phone, email, internet, or mail; Analyze caller questions and formulate accurate responses using approved resources; Identify, record, and triage adverse events and product complaints; Maintain knowledge of client products, SOPs, protocols, GCPs, and regulatory requirements; Research medical literature and draft responses for complex inquiries.
Seniority
Entry-level to Mid-level