Job Description
Join to apply for the Drug Safety Specialist role at Planet Pharma
Join to apply for the Drug Safety Specialist role at Planet Pharma
Position Summary
The Drug Safety Specialist is primarily responsible for case processing of serious adverse events, serious and non-serious adverse drug reactions and other medically related project information such as adverse events of special interest and product complaints.
Job Description
Pay range: 61-64/hr
depending on experience
DRUG SAFETY SPECIALIST
Position Summary
The Drug Safety Specialist is primarily responsible for case processing of serious adverse events, serious and non-serious adverse drug reactions and other medically related project information such as adverse events of special interest and product complaints.
This position is fully remote.
Essential Duties And Responsibilities
Reviews, processes, and assesses adverse event reports (AERs) from clinical trials and post-marketing sources
Enters and maintains safety data in the global safety database
Prepares and submits safety reports to regulatory authorities in accordance with global safety reporting requirements
Performs QC of cases to ensure quality levels are maintained per DOB’s expectations
Manages the safety intake mailbox including the triage of incoming reports for completeness, legibility, and validity
Query management
Maintains electronic documentation for case files within the safety database
Assists with reconciliation of the safety and clinical trial databases
Collaborates with cross-functional teams to ensure timely and accurate reporting of adverse events to regulatory agencies
Adheres to all relevant pharmacovigilance regulations and company policies
Assists in development of project-specific safety procedures, workflows, and templates.
Assists in project-specific safety database setup, management of data entry guidelines, and user acceptance testing.
MedDRA and WHODrug coding in the safety database
Preparation for, participation in, and follow-up on audits and inspections
Provides training and guidance to colleagues on drug safety processes and procedures.
Stays updated on industry developments and changes in drug safety regulations.
Maintains confidentiality and adheres to ethical standards in handling sensitive and confidential information.
Performs other duties and responsibilities as assigned by management.
Qualifications
Degree in Pharmacy, Nursing, Life Science, or other fields, or equivalent qualification/work experience
The ideal candidate will have 2+ years of recent case processing experience and must include experience processing post-marketing cases
MedDRA and WHODrug coding experience
Must be fluent in English with excellent written and verbal communication skills
Detail orientated and capable of working effectively within a team environment.
Excellent organizational and prioritization skills
Analytical and problem-solving skills
Able to perform database/literature searches
Experience working in RxLogix’s Pharmacovigilance Case Management system a plus
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Seniority level Seniority level Not Applicable
Employment type Employment type Full-time
Job function Job function Management and Manufacturing
Industries Staffing and Recruiting
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Job Tags
Full time, Contract work, Work experience placement,