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Pharmacovigilance and Clinical Research @ Resolve

Home > Back Office OperationsQuality (QA-QC)

 Pharmacovigilance and Clinical Research

Job Description

Typical responsibilities include:

  • Recording and reporting adverse reactions received from healthcare professionals and consumers
  • Conducting in-depth interviews with patients and healthcare professionals
  • Developing a thorough knowledge of products completing periodic safety update reports on drugs and other treatments
  • Writing and reviewing serious adverse effects reports and forms flagging up
  • Early warning signs of adverse effects of drugs minimizing the risk of serious side effects completing safety audits working on clinical trials of new drugs
  • Ties including site initiations, monitoring and close-outs at clinical trial sites for low to medium risk/complexity studies.

Description Track all adverse event reports received and completed Review and assess all source documents and compile data in an adverse event report Data enter report into the client safety database Code adverse events in the client safety database Release report to client through client safety database

Regards

Sonali

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Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Back Office OperationsQuality (QA-QC)
Functional Area: Not Applicable
Role/Responsibilies: Pharmacovigilance and Clinical Research

Contact Details:

Company: Resolve Itech Corp
Location(s): Multi-City, India

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Keyskills:   good clinical practice medical research clinical operations clinical trial management system clinical trials clinical research pharmacovigilance

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₹ 3.5 - 5 Lakh/Yr

Resolve

Resolve ITech Corp Providing DHA HAAD MOH PROMETRIC NCLEX FPGEE KAPS PEBC USMLE Coaching for Healthcare Professionals Our unique training methodology helps the aspirants to achieve their goal at ease. Before Initiating the practice in any healthcare facility in overseas i.e., Dubai, Abudhabi, UAE, O...