Data Officer – ProductLife Group Remote Job | Pharmacovigilance Data Entry

Data Officer – ProductLife Group Remote Job | Pharmacovigilance Data Entry | 2+ Years Experience Apply Now ProductLi...

Data Officer – ProductLife Group

Remote Job | Pharmacovigilance Data Entry | 2+ Years Experience

Apply Now

ProductLife Group (PLG) is hiring for the position of Data Officer (IN). This is a remote opportunity for professionals with experience in pharmacovigilance data entry, Individual Case Safety Reports (ICSRs), and XEVMPD activities.

The role is particularly suited to candidates with an academic background in Life Sciences, Pharmacy, Biotechnology, Biology or a related scientific discipline who have practical experience working with pharmacovigilance cases and safety data.

Job Highlights

• Position: Data Officer (IN)
• Company: ProductLife Group
• Work Mode: Remote
• Minimum Experience: 2 Years
• Employment: Contractual / Temporary or Permanent
• Field: Pharmacovigilance / Life Sciences
• ICSR Processing Experience Required
• XEVMPD Experience Required

Job Overview

Company	ProductLife Group (PLG)
Job Title	Data Officer (IN)
Work Mode	Remote
Employment Type	Contractual / Temporary / Permanent
Experience	Minimum 2 Years in Pharmacovigilance Data Entry
Education	Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Biology or Related Discipline
Salary	Not Specified in the Provided Listing
Location	Remote, India

About ProductLife Group

ProductLife Group is a global consulting and outsourcing organization that supports companies in the life sciences industry throughout the product lifecycle.

The Data Officer position forms part of the organization's pharmacovigilance operations, where accurate handling of safety information and regulatory case data is essential.

About the Data Officer Role

The Data Officer will be responsible for handling pharmacovigilance cases and maintaining accurate safety information. The role involves reviewing and entering safety data, processing Individual Case Safety Reports, supporting regulatory submissions and ensuring compliance with applicable procedures and quality standards.

The position requires strong attention to detail because pharmacovigilance data must be accurate, complete and consistent across safety databases.

Key Responsibilities

• Perform triage, review and data entry of pharmacovigilance cases.
• Process and maintain Individual Case Safety Reports (ICSRs).
• Ensure case processing follows applicable regulations and internal procedures.
• Support submission of ICSRs to health authorities, clients and partners.
• Manage and monitor assigned pharmacovigilance mailboxes.
• Follow up with consumers, patients, healthcare professionals and other stakeholders to obtain missing safety information when required.
• Perform XEVMPD-related activities.
• Maintain accuracy, completeness and consistency of safety data.
• Follow quality standards, SOPs and regulatory requirements.
• Work with cross-functional teams and external/internal stakeholders.
• Support continuous improvement and operational excellence initiatives.

Educational Qualification

Candidates should have a Bachelor's degree in one of the following fields or a related scientific discipline:

• Life Sciences
• Pharmacy
• Biotechnology
• Biology
• Related Scientific Discipline

Experience Required

Minimum Experience: 2 Years

Candidates must have at least 2 years of experience in pharmacovigilance data entry within a post-marketing environment.

• Experience handling and processing ICSRs.
• Practical experience with XEVMPD activities.
• Experience with pharmacovigilance databases is preferred.
• Knowledge of safety database management systems is an advantage.
• Previous experience with XEVMPD maintenance and data management is preferred.

Technical Skills

• Microsoft Word
• Microsoft Excel
• Microsoft Outlook
• Microsoft PowerPoint
• Pharmacovigilance databases
• Safety database management systems
• XEVMPD

Required Language Skills

• Excellent written English.
• Excellent verbal communication skills in English.
• Knowledge of additional languages may be an advantage.

Key Competencies

• Attention to Detail
• Customer Focus
• Accountability
• Teamwork and Collaboration
• Communication Skills
• Problem Solving
• Planning and Organization
• Quality Orientation

Preferred Qualifications

• Experience working with pharmacovigilance databases.
• Knowledge of regulatory pharmacovigilance requirements.
• Exposure to safety database management systems.
• Additional experience with XEVMPD maintenance.
• Experience in safety data management.
• Database experience.

The listing also indicates that training may be provided where needed for certain database-related activities.

Who Should Apply?

This role is best suited to professionals who already have experience in pharmacovigilance rather than entry-level data entry candidates. Applicants should have relevant scientific education and practical experience processing safety cases and ICSRs.

• Pharmacovigilance professionals.
• Drug safety professionals.
• Life sciences graduates with relevant PV experience.
• Pharmacy graduates with pharmacovigilance experience.
• Professionals experienced in ICSR processing.
• Candidates with XEVMPD experience.

Work From Home Opportunity

The position is listed as Remote, allowing eligible candidates to work remotely from India. Candidates should ensure they have the appropriate setup and connectivity required for professional remote work.

Salary & Employment Terms

The supplied job listing does not mention a specific salary range. The position is listed under Contractual / Temporary and Permanent employment types. Candidates should confirm the applicable compensation and employment terms during the recruitment process.

How to Apply?

Interested and eligible candidates can apply through the official Indeed job listing. Make sure your resume clearly highlights your pharmacovigilance, ICSR processing and XEVMPD experience.

Apply for Data Officer

Frequently Asked Questions

What is the job role?

The position is Data Officer (IN) with ProductLife Group.

Is this a remote job?

Yes. The position is listed as a Remote opportunity.

How much experience is required?

A minimum of 2 years of pharmacovigilance data entry experience in a post-marketing environment is required.

Is ICSR experience required?

Yes. Experience handling and processing Individual Case Safety Reports (ICSRs) is required.

Is XEVMPD experience required?

Yes. The listing specifically requires proven experience with XEVMPD activities.

What educational qualification is required?

A Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Biology or a related scientific discipline is required.

Is this suitable for freshers?

No. The listing requires a minimum of 2 years of relevant pharmacovigilance experience.

What is the salary?

The salary is not specified in the supplied job listing. Candidates should confirm compensation during the hiring process.

Disclaimer: This job information is prepared from the supplied Indeed listing for informational purposes. We are not the recruiter or hiring agency. Salary, employment type, eligibility, responsibilities and other conditions may change. Candidates should verify the latest information on the official job listing before applying. Never pay a recruitment fee to obtain a job.