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Data Officer – Clinical Safety (Remote)

Fresher years
3-5 LPA
15 Feb. 27, 2025
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Job Opportunity: Data Officer – Clinical Safety (Remote) | ProductLife Group

Position: Data Officer – Clinical Safety
Location: India (Remote Work Possible)
Department: Life Cycle – Safety and Vigilance
Job Type: Permanent Contract
Company: ProductLife Group

 

Role Overview:

ProductLife Group is seeking a Data Officer – Clinical Safety to support pharmacovigilance activities within our dynamic team. The selected candidate will be responsible for processing adverse event data, maintaining clinical safety records, and ensuring compliance with regulatory requirements.

 

Key Responsibilities:

  • Adverse Event (AE) & Serious Adverse Event (SAE) Processing: Manage SUSARs and other immediately reportable events in the safety database, ensuring accurate and timely communication with customers.

  • Query Management: Prepare, send, and follow up on queries related to case processing.

  • Study Trackers Maintenance: Maintain and update study trackers and relevant pharmacovigilance tools.

  • Clinical Safety Reconciliation: Collaborate with CROs, data management teams, and customers to reconcile clinical safety data.

  • Aggregate & Periodic Safety Reports: Assist in the preparation and submission of expedited and periodic safety reports.

 

Eligibility Criteria:

  • Education: Bachelor’s degree (BSc) in Life Sciences or PharmD (Doctor of Pharmacy).

  • Experience:

    • 0–2 years of experience in pharmacovigilance/drug safety data entry (Fresh graduates with relevant training/internships are encouraged to apply).

    • Understanding of safety databases (e.g., SafetyEasy) is preferred.

    • Knowledge of drug safety regulations (national & international).

    • Familiarity with the pharmaceutical industry and pharmacovigilance tools.

  • Case Management: Hands-on experience in case processing and management (via internships or training programs is a plus).

 

Required Skills:

  • Strong analytical and problem-solving skills.

  • Adaptability and ability to work in a fast-paced environment.

  • Excellent written communication and documentation skills.

  • Proficiency in MS Office and pharmacovigilance software.

  • Reliability, attention to detail, and a proactive mindset.

 

Why Join ProductLife Group?

  • Opportunity to work remotely in a global pharmaceutical safety environment.

  • Competitive salary and benefits package.

  • Professional growth in clinical safety and pharmacovigilance.

 

How to Apply?

Interested candidates can submit their resume and a cover letter detailing their qualifications and interest in the role.

 

🚀 Fresh graduates with relevant education and training are encouraged to apply!


Join ProductLife Group and contribute to ensuring drug safety and patient well-being worldwide!