Adverse Events, Biotech and Pharmaceutical, Computer Skills, Data Entry, Data Quality, Detail Oriented, Editing, Healthcare, Investigational New Drug (IND), Medical Coding, Organizational Skills, Pharmacovigilance, Presentation/Verbal Skills, Problem Solving Skills, Product Marketing, Product Safety, Proofreading, Standard Operating Procedures (SOP), Writing Skills
Job Location: Nutley, NJ (100% REMOTE)
Job Duration: 12 Months+ Possible Extension
Shift: Monday - Friday 37.5 hours per week
Payrate: $27.00/ hr. on w2
This position is within the Product Safety Group.
Description of Responsibilities:- Code and enter information into the Product Safety database for Adverse Events reported in association with client’s Marketed and investigational products.
- The individual will be responsible for verifying the accuracy and completeness of information for each adverse event report for which he/she is assigned in conjunction with the source documents and ensuring that the activities are performed in a manner consistent with SOPs.
Requirements:- Health Care Professional (with or without previous drug safety experience) or non-health Care Professional with previous drug safety experience desired
- 2-3 year’s minimum experience in medical coding/terminology within a pharmaceutical organization.
- Computer proficiency required, including data entry of adverse event information into standardized electronic databases such as ARISG/ARGUS
- Strong written and verbal communications are essential
- Strong attention to detail and accuracy are essential
- Strong proofreading, editing and reviewing skills are essential
- Must be able to work independently, and possess problem solving skills, but also know when to seek assistance from manager.
- Bachelor's Degree Required.
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Integrated Resources, Inc