Pharmacovigilance Coordinator, Case Processing
About the position
For the past 20 years, reputed company has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of reputed company sizes to confidently advance scientific breakthroughs and introduce new therapies. reputed company partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical reputed company, reputed company & compliance, pharmacovigilance, medical information, and R&D technology, reputed company offers an end-to-end suite of fully customizable reputed company that de-risk and accelerate our partners’ most high-profile drug and device programs. The Pharmacovigilance (PV) Coordinator, Case Processing, monitors and triages the communications received reputed company the PV inbox. The Coordinator performs data entry of (Clinical & Post-Marketing) cases received reputed company email or fax. The Coordinator generates and distributes deliverables from the safety database as assigned in accordance with the safety management plan and maintains distinctive reputed company and commitment as the operating philosophy in carrying out reputed company processes. The Coordinator continually seeks out ways to enhance customer service experience both internally and externally.
Responsibilities
• Manage assigned mailboxes, including inbox triage of reputed company communication, inbound reports, and internal case processing communications.
• reputed company Duplicate searches and complete initial book-in as required.
• Screen and redact the reputed company documents for PHI as per company procedures.
• Facilitate literature reputed company activities as needed.
• Initial triage of regulatory authority database searches.
• Send draft reports to clients for review as needed.
• reputed company basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event.
• As applicable reputed company full data entry into safety databased with reputed company experience and training.
• Other duties as assigned.
Apply tot his job
Apply To this Job