ProductLife Group Hiring Data Officer (Pharmacovigilance)

ProductLife Group Hiring Data Officer (Pharmacovigilance) | Pharmacy & Life Sciences | Remote

Pharmacovigilance professionals seeking remote healthcare and drug safety careers have an excellent opportunity with ProductLife Group (PLG). The company is currently hiring for the position of Data Officer (Pharmacovigilance) to support global drug safety operations and vigilance activities. This remote role offers the chance to work with international clients while contributing to adverse event reporting, case processing, safety database management, and pharmacovigilance compliance activities.

Candidates with experience in Individual Case Safety Report (ICSR) processing, pharmacovigilance data entry, quality control review, and global drug safety regulations can explore this opportunity to advance their careers within a leading life sciences and regulatory services organization.

Company Overview

ProductLife Group (PLG) is a global provider of regulatory affairs, pharmacovigilance, quality compliance, and life cycle management services for pharmaceutical, biotechnology, and healthcare companies. The organization supports clients throughout the product lifecycle, helping ensure regulatory compliance, patient safety, and successful market access across multiple regions.

With operations spanning several countries, ProductLife Group delivers specialized services in drug safety, regulatory strategy, medical information, quality assurance, and vigilance activities. The company continues to expand its global pharmacovigilance operations to support increasing regulatory requirements and patient safety initiatives worldwide.

Job Role & Responsibilities

Position: Data Officer (Pharmacovigilance)

The selected candidate will support pharmacovigilance case management activities and ensure compliance with global drug safety reporting requirements.

Key Responsibilities

• Perform safety case receipt, processing, and pharmacovigilance data entry activities.
• Manage Individual Case Safety Reports (ICSRs) according to client requirements and regulatory timelines.
• Conduct quality control tracking and follow-up activities for safety cases.
• Manage generic and client-specific pharmacovigilance email inboxes.
• Register, triage, assign, and coordinate vigilance case processing activities.
• Follow up with healthcare professionals, reporters, and relevant stakeholders for additional safety information.
• Respond to client and reporter queries related to pharmacovigilance cases.
• Perform periodic reconciliations to ensure accurate handling of vigilance reports.
• Support local pharmacovigilance activities and safety operations.
• Participate in audits, inspections, and implementation of corrective actions.
• Maintain compliance with global pharmacovigilance regulations and internal procedures.

Eligibility / Qualifications

Educational Qualification

Candidates should possess:

• Bachelor’s Degree in Pharmacy
• Master’s Degree in Pharmacy
• Nursing
• Medicine
• Life Sciences
• Biomedical Sciences
• Other relevant healthcare or science-related qualifications

Relevant Courses

B.Pharm, M.Pharm, Pharm.D, Nursing, MBBS, Life Sciences, Biotechnology, Microbiology, Biochemistry, Biomedical Sciences, Clinical Research, Pharmacology, Toxicology, Healthcare Management.

Experience Required

• Minimum 2+ years of Pharmacovigilance experience
• Experience in ICSR processing and pharmacovigilance data entry
• Experience working with service providers or pharmacovigilance operations preferred

Required Skills

• Pharmacovigilance case processing
• ICSR management
• Adverse event reporting
• Safety database operations
• Quality control review
• Client communication
• Drug safety compliance
• GVP knowledge
• GCP understanding
• FDA regulations awareness
• EU pharmacovigilance regulations
• Case follow-up management
• Data reconciliation
• Regulatory compliance

Location & Salary

Location: Remote (India)

Salary: ₹6 LPA – ₹10 LPA (Approximate)

Application Process

Interested candidates can apply through the official LinkedIn job posting.

Apply Here: https://www.linkedin.com/jobs/view/4420140630/

Job Information

• Company: ProductLife Group
• Position: Data Officer (Pharmacovigilance)
• Work Mode: Remote
• Time Zone: Eastern USA Time Zone
• Experience: 2+ Years
• Industry: Pharmacovigilance / Drug Safety

Frequently Asked Questions (FAQs)

1. What qualification is required for the Data Officer role?

Candidates with Pharmacy, Life Sciences, Nursing, Medicine, or related healthcare qualifications are eligible to apply.

2. Is this a remote opportunity?

Yes. This is a remote work opportunity based in India.

3. How much experience is required?

Applicants should have at least 2 years of pharmacovigilance experience.

4. What pharmacovigilance activities will be handled?

The role includes ICSR processing, adverse event reporting, safety case management, quality control review, reconciliations, and follow-up activities.

5. Is knowledge of global pharmacovigilance regulations required?

Yes. Candidates should have knowledge of GVP, GCP, FDA regulations, EU pharmacovigilance requirements, and drug safety reporting processes.

6. What work schedule will be followed?

Candidates will be required to work according to the Eastern USA Time Zone.

Summary Table

Company	ProductLife Group
Department Vacancies	Data Officer (Pharmacovigilance)
Qualification	B.Pharm, M.Pharm, Pharm.D, Nursing, Medicine, Life Sciences, Biotechnology, Microbiology
Experience	2+ Years
Location	Remote (India)