An amazing chance to work in an exceptionally expertise in consulting solutions to the various global companies. You will review, find and entre Adverse Event data from products and reports from various sources in compliance with existing procedures. Our client is looking to hire an individual with in-depth understanding of medical and life sciences in pharmacovigilance.
If this sounds exciting please apply with us!
Your Employer: A leading, global firm providing creative and strategic analytics, IT and consulting solutions for the entire enterprise value chain.
You will be Responsible For:
Reviewing, extracting and entering Adverse Event data from the various authentic sources in accordance with defined procedures.
Interpret case related information including AE coding, lab results and other procedures along with compiling narrative summaries.
Punctuality for re-portable cases preparation and reporting.
Review and verify follow up information for the cases.
Contributions to the projects and case processing information and systems.
Mentor staff in pharmacovigilance methodology and in case processing.
The Successful Candidate:
Bachelors/Masters in Medical/ Pharmaceutical/ Life Sciences.
2-6 years of experience in clinical research domain.
In-depth understanding of Medical and Life Sciences.
Extensive experience in Pharmacovigilance.
Understanding of the principles and concepts with Patient safety case processes.
Knowledge and understanding GCP Guidelines.
What is in it for you?
Exceptional career growth.
Opportunity to work with globally competitive firm.
If you find this role adding value in your career, kindly write me an email along with your updated CV on email@example.com for a confidential discussion on the role.