Pharmacovigilance Job at ProPharma | B Pharm Graduates | Apply Now
Searching for a rewarding Pharmacovigilance Job in the pharmaceutical industry? ProPharma is hiring a Pharmacovigilance Scientist for its global Benefit-Risk team in India. This excellent B Pharm Job opportunity is ideal for candidates with experience in drug safety, aggregate report writing, signal management, and literature screening. Candidates looking to build a strong career in pharmacovigilance and global regulatory compliance should not miss this opportunity.
- Job Position: Pharmacovigilance Scientist
- Location: India (Remote Role)
- Job ID: JR 9433
About the Company
ProPharma has improved the health and wellness of patients for over 20 years by supporting biotech, pharmaceutical, and medical device organizations with expert consulting solutions. The company specializes in regulatory sciences, clinical research, pharmacovigilance, medical information, quality compliance, and R&D technology services.
Job Description
ProPharma is seeking a dedicated and detail-oriented Pharmacovigilance (PV) Safety Scientist to support key pharmacovigilance activities and ensure compliant delivery of safety and regulatory outputs.
This Pharmacovigilance Job is suitable for candidates with expertise in aggregate safety reports, signal management, literature review, and global PV compliance. The role is also an excellent B Pharm Job opportunity for pharmacy graduates aiming to advance their careers in drug safety and regulatory affairs.
Key Responsibilities
- Author aggregate safety reports, including:
- PSURs / PBRERs
- PADERs / Annual Reports / ACO
- DSURs
- Prepare and maintain Risk Management Plans (RMPs)
- Author and contributor to Signal Management Reports
- Conduct literature searches, screening, and validity checks
- Perform duplicate checks and literature review using appropriate tools
- Extract and validate safety data, including RSI, sales data, prior reports, and signals
- Generate and review line listings (LLs) from safety databases
- Reconcile and maintain process trackers
- Support high-priority and ad hoc pharmacovigilance activities
- Ensure compliance with global regulatory requirements and timelines
- Participate in audits and inspections as a Subject Matter Expert (SME)
- Contribute to SOP/WI development, deviations, and CAPAs
Qualifications
Candidates should possess a Bachelor’s or Master’s degree in:
- Pharmacy
- Related healthcare or scientific field
Equivalent experience may also be considered.
Experience
- Minimum 2+ years of Pharmacovigilance experience
- Experience in:
- Medical writing and aggregate reports
- Literature search and screening
- Signal detection
- Experience in authoring and reviewing aggregate safety reports
- Exposure to quality metrics and client-facing discussions is desirable
Skills Required
- Strong analytical and problem-solving abilities
- Excellent attention to detail
- Effective organizational and time management skills
- Strong written and verbal communication skills
- Ability to interpret scientific data clearly and concisely
- Understanding of ICH-GCP, FDA, EMA, and global PV regulations
- Proficiency in MS Office and web-based applications
