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Pharmacovigilance Specialist

Clinovo
Clinovo
3-5 years
Not Disclosed
10 Sept. 23, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Hiring: Pharmacovigilance Specialist

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!


Key Responsibilities:

  • 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.


Requirements:

  • 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.