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Pharmacovigilance Associate

0-1 years
Not Disclosed
10 March 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Veeda Lifesciences is Hiring FRESHERS for Pharmacovigilance Associate

About the Company:
Veeda Lifesciences is a leading independent Clinical Research Organization (CRO) specializing in the delivery of clinical research solutions to global pharmaceutical, biotechnology, and medical device companies. The organization is known for its high ethical standards, quality processes, and dedication to delivering accurate and reliable clinical data.

Job Title: Pharmacovigilance Associate
Job Location: Ahmedabad
Experience: 0-1 year
Qualification:

  • B.Pharm, M.Pharm, or relevant field in Life Sciences or Allied Fields

  • Basic understanding of pharmacovigilance principles, regulatory requirements, and drug safety processes is preferred but not mandatory.

Employment Type: Hybrid (Combination of on-site and remote work based on project requirements)

Key Responsibilities:

  • Perform case processing activities including case intake, data entry, narrative writing, and quality control.

  • Assess and process adverse event information reported from clinical trials, post-marketing surveillance, and literature.

  • Monitor, track, and ensure compliance with regulatory timelines and reporting requirements.

  • Prepare and submit Individual Case Safety Reports (ICSRs) and periodic safety reports to regulatory authorities.

  • Assist with signal detection activities and contribute to risk management strategies.

  • Collaborate with cross-functional teams to ensure compliance with pharmacovigilance regulations.

Required Skills:

  • Strong analytical and critical thinking skills.

  • Good knowledge of medical and scientific terminology.

  • Excellent written and verbal communication skills.

  • Attention to detail and the ability to manage multiple tasks effectively.

  • Basic knowledge of regulatory guidelines such as ICH-GCP and pharmacovigilance reporting requirements.

Benefits:

  • Hands-on training and exposure to pharmacovigilance processes.

  • Opportunity to work with a globally recognized organization.

  • Competitive salary and growth opportunities.

  • Supportive work environment promoting continuous learning and professional development.

Interested Candidates:
Share your resumes at
Vaibhav.D3662@veedalifesciences.com