Location: Bangalore, Kochi, Thane, Pune, Kolkata (Hybrid Mode)
Are you a passionate Pharmacovigilance Specialist with expertise in Argus and case processing? Join our team and make a positive impact on patient safety!
End-to-End Case Processing:
Conduct data entry, medical assessment, and quality review for adverse event reports.
Adverse Event Management:
Utilize Argus for effective management of adverse event reports.
Legal Case Processing:
Ensure compliance with global regulations in legal case processing.
Collaboration:
Work closely with cross-functional teams and regulatory authorities.
Regulatory Updates:
Stay informed about pharmacovigilance regulations and industry best practices.
Experience:
3-5 years in Pharmacovigilance with hands-on experience in Argus and case processing.
Legal Knowledge:
Familiarity with legal case processing and global regulatory frameworks (FDA, EMA, etc.).
Skills:
Proficient in Argus, case processing, legal case processing, quality review, and GVP.
Interested?
Send your resume to Maneesha.p@clinovo.com
For more information, visit us at www.clinovo.com.
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Bangkok |