PLG Remote Hiring Pharmacovigilance Data Officer

ProductLife Group (PLG) is hiring for the position of Data Officer – Pharmacovigilance in India. This is a work-from-home opportunity for candidates with relevant experience in pharmacovigilance, drug safety, case processing, regulatory affairs, or safety database management.

The role involves managing and processing vigilance cases, maintaining safety data, performing database activities, preparing reports, supporting regulatory submissions, and contributing to quality and process improvement initiatives.

Candidates with qualifications such as B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Nursing, Dentistry, or a related scientific degree may be eligible. The vacancy indicates 1–3 years of experience and an advertised compensation of up to ₹5.5 LPA.

ProductLife Group Recruitment 2026 – Job Highlights

ParticularsDetails
CompanyProductLife Group (PLG)
Job TitleData Officer – Pharmacovigilance
Job LocationIndia – Remote
Work ModeWork From Home
Employment TypeNot specified in the provided details
Experience1–3 Years
QualificationB.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Nursing, Dentistry or related
DepartmentPharmacovigilance / Drug Safety
Key SkillsCase Processing, MedDRA, EudraVigilance, Safety Databases
Advertised SalaryUp to ₹5.5 LPA
Application ModeOnline

About ProductLife Group

ProductLife Group (PLG) is a global consulting and outsourcing organization focused on the life sciences industry. The company supports organizations across areas associated with the product lifecycle, including development, clinical research, regulatory activities, market access, and product safety.

PLG works with organizations across sectors such as pharmaceuticals, biotechnology, medical devices, cosmetics, and nutrition.

Job Description

The Data Officer – Pharmacovigilance will support the management of safety and vigilance data throughout relevant operational processes.

The position involves receiving and registering cases, conducting duplicate checks, performing initial case assessment and data entry, coding medical information, preparing case narratives, managing follow-ups, and supporting case submissions.

The role also includes safety database reporting, regulatory activities, KPI monitoring, reconciliation, quality checks, and process improvement.

Educational Qualification

Candidates with the following educational backgrounds may be considered:

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • B.Sc
  • M.Sc
  • Life Sciences
  • Nursing
  • Dentistry
  • Related scientific disciplines

The qualification should provide a relevant foundation for pharmacovigilance, drug safety, medical information, or related life sciences activities.

Experience Requirements

The vacancy is listed for candidates with 1–3 years of experience.

Relevant professional experience may include:

  • Pharmacovigilance
  • Drug Safety
  • Safety Case Processing
  • Regulatory Affairs
  • Safety Database Management
  • Vigilance Data Management

Candidates with direct experience in safety case processing and pharmacovigilance operations may find their background particularly relevant to the role.

Required Technical Skills

Candidates should have knowledge or experience in areas such as:

  • Pharmacovigilance case processing
  • Vigilance data management
  • MedDRA coding
  • EudraVigilance
  • Safety database operations
  • Data entry and database management
  • Regulatory reporting
  • Microsoft Office
  • KPI and activity reporting
  • Data reconciliation
  • Quality and compliance processes

Knowledge of pharmacovigilance regulations and safety databases is preferred.

Key Responsibilities

1. Vigilance Case Processing

The selected candidate will support day-to-day vigilance case management activities, including:

  • Monitoring shared and client-specific mailboxes for incoming safety information.
  • Registering vigilance cases in internal tracking systems.
  • Performing duplicate searches within safety databases.
  • Conducting initial case triage.
  • Entering relevant case information accurately.
  • Coding medical information using MedDRA.
  • Preparing and updating case narratives.
  • Applying patient-data anonymization requirements where necessary.
  • Supporting follow-up activities.
  • Assisting with case closure.
  • Assessing case seriousness and applicable reporting requirements.

2. Safety Database Management

The role involves maintaining and working with safety databases.

Responsibilities may include:

  • Performing database searches.
  • Extracting safety information and data.
  • Generating reports and data listings.
  • Supporting database quality checks.
  • Contributing to reconciliation activities.
  • Maintaining accurate and complete safety records.

3. Reporting and KPI Monitoring

The Data Officer will support operational reporting activities such as:

  • KPI calculations
  • Activity monitoring
  • Weekly reports
  • Monthly reports
  • Quarterly reports
  • Annual activity reports
  • Safety database listings

The candidate will be expected to maintain accurate information for operational monitoring and reporting.

Regulatory Activities

The role includes supporting several pharmacovigilance and regulatory activities.

EudraVigilance

The selected candidate may support:

  • ICSR downloads
  • ICSR submissions
  • Related EudraVigilance activities

XEVMPD

Responsibilities may also include:

  • XEVMPD data updates
  • XEVMPD submissions

Health Authority Reporting

The position may support reporting activities involving:

  • MHRA
  • FDA
  • Other applicable Health Authorities

Specific reporting responsibilities may depend on project and client requirements.

Quality and Compliance

Quality and regulatory compliance are important components of the role.

The Data Officer will support:

  • Compliance with applicable pharmacovigilance regulations.
  • Adherence to company procedures.
  • Maintenance of accurate safety records.
  • Quality checks and reconciliation activities.
  • Audit and inspection support.
  • Appropriate documentation of operational activities.

Process Improvement and Client Projects

The selected candidate may participate in activities designed to improve pharmacovigilance operations.

Responsibilities include:

  • Supporting implementation of new client projects.
  • Participating in process optimization initiatives.
  • Helping improve operational workflows.
  • Drafting and updating work instructions.
  • Supporting technical agreement updates.
  • Assisting with operational procedure development and maintenance.

Soft Skills

The role requires a combination of analytical, organizational, and communication skills.

Candidates should have:

  • Strong attention to detail
  • Good organizational abilities
  • Critical-thinking skills
  • Analytical approach
  • Effective written and verbal communication
  • Ability to work collaboratively
  • Ability to manage multiple priorities
  • Good time-management skills
  • Ability to meet deadlines
  • Quality-focused mindset

Work Location and Work From Home

Location: India

Work Mode: Remote / Work From Home

The vacancy is advertised as a remote India opportunity. Candidates should confirm any specific working-hour, availability, or project-related requirements during the recruitment process.

Salary / CTC

The vacancy information lists an advertised salary of up to ₹5.5 LPA.

The actual compensation offered to an individual candidate may depend on factors such as qualifications, relevant experience, role requirements, and the employer’s offer.

What ProductLife Group Offers

The vacancy highlights the following aspects of the opportunity:

  • Exposure to an international Life Sciences environment.
  • Experience with global pharmacovigilance and regulatory activities.
  • Professional development opportunities.
  • Career growth exposure.
  • Collaborative working environment.

Specific employment benefits and terms may vary according to the applicable employment conditions.

Selection Process

A detailed selection process has not been specified in the provided vacancy information.

Candidates may be evaluated based on their:

  • Educational qualifications
  • Pharmacovigilance experience
  • Case-processing knowledge
  • MedDRA knowledge
  • Safety database experience
  • Regulatory knowledge
  • Communication skills
  • Analytical and organizational abilities

The exact recruitment stages should be confirmed by ProductLife Group.

How to Apply for ProductLife Group Recruitment 2026

Interested and eligible candidates can apply online through the official ProductLife Group careers page.

Candidates should submit accurate information regarding their education and professional experience and ensure that their resume reflects relevant pharmacovigilance or drug safety experience.

Important Details Before Applying

  • Position: Data Officer – Pharmacovigilance
  • Company: ProductLife Group (PLG)
  • Location: India – Remote
  • Work arrangement: Work From Home
  • Experience: 1–3 years
  • Relevant backgrounds: Pharmacy, Life Sciences, Nursing, Dentistry and related scientific fields
  • Important skills: Pharmacovigilance, MedDRA, EudraVigilance, safety databases and regulatory reporting
  • Advertised salary: Up to ₹5.5 LPA
  • Application mode: Online
  • Candidates should review the official vacancy before submitting their application.

Frequently Asked Questions

1. What is the job title at ProductLife Group?

The position is Data Officer – Pharmacovigilance.

2. Which company is hiring for this role?

The hiring organization is ProductLife Group (PLG).

3. Where is the job located?

The position is listed for India – Remote.

4. Is this a work-from-home job?

Yes. The vacancy is advertised as a remote/work-from-home opportunity in India.

5. How much experience is required?

The vacancy specifies 1–3 years of experience.

6. What qualifications are accepted?

The listed backgrounds include B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Nursing, Dentistry, and related scientific fields.

7. What are the major responsibilities?

Major activities include vigilance case processing, MedDRA coding, safety database management, case narratives, follow-ups, regulatory reporting, KPI reporting, reconciliation, and quality activities.

8. Is MedDRA knowledge required?

MedDRA coding is listed among the technical skills relevant to the position.

9. What salary is mentioned for this job?

The vacancy advertises compensation of up to ₹5.5 LPA. The final offer may vary based on the candidate and employment terms.

10. How can candidates apply?

Candidates can apply online through the official ProductLife Group job listing using the application link provided above.

Important Note

Recruitment requirements, vacancy status, compensation, work arrangements, and employment conditions may change. Candidates should verify the latest information on the official ProductLife Group careers page before applying. The advertised salary of ₹5.5 LPA should be understood as a stated upper figure rather than a guaranteed salary for every selected candidate. Application submission does not guarantee selection or employment.

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