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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.
Summary of Responsibilities:
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.
Summary of Responsibilities:
- Segregate cases received as per priority and due dates in the database worklist.
- Assign cases to case processing team based on the priority and availability of resources in consultation with Team Lead or designee.
- Enter data into the Master case tracking sheet. Track and monitor the case progression with help of case tracking sheet. Follow up with associates and/or team leads to ensure timely completion of review and ensure case prioritization.
- Reconciliation of TAT data on a daily basis to ensure all the cases are assigned and reviewed as per SLA.
- Ensure timely updating of productivity, QC and other role specific trackers on a real time basis and follow up with Team Leads for the same.
- Daily reconciliation of received and processed cases to ensure all received cases is processed with internal timelines.
- Perform any other Pharmacovigilance support activities as assigned – tracking various types of information and metrics, reconciliation of data from multiple sources.
- Bachelor's degree preferably healthcare related
- Minimum 6 months of relevant experience
- Must be amenable to work on a hybrid work setup and night shift schedule
- Understanding of Pharmacovigilance preferable.
- Good understanding of safety database.
- Technical proficiency with Microsoft Office suite of applications (including hands on experience in Excel Macro programming preferred)
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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