Career Opportunity for Pharma Candidates: Senior Pharmacovigilance Associate Job at Quanticate | Apply Now
Join Quanticate, a world-leading data-focused CRO, as a Senior Pharmacovigilance Associate and contribute to global clinical trials and pharmaceutical safety. This role offers the opportunity to work with top pharmaceutical and biotech companies, ensuring compliance with pharmacovigilance regulations and advancing drug safety. If you have experience in ICSR processing, safety data management, and a strong understanding of ICH GCP, this could be your next career move. Apply now to be part of an innovative and growing team at Quanticate!
Job Title: Senior Pharmacovigilance Associate
Key Duties of Role:
- Assist with the processing of cases (Spontaneous, literature, and clinical) as required in compliance with applicable regulations and Quanticate SOPs.
- Triage of cases for completeness, accuracy, and redaction.
- Entry of safety data onto the safety databases and tracking systems.
- Coding of adverse events, medical history, and medications.
- Assist with weekly and ad-hoc global literature searches.
- Support the Pharmacovigilance Lead on assigned projects as appropriate.
Requirements:
- Education: Pharmacy, life science, or healthcare degree.
- Desirable: Higher degree or medical qualification.
- Minimum 2 years of experience in ICSR processing, safety data management, and safety data entry.
- Knowledge of ICH GCP and other relevant regulations and guidelines.
- Good organizational and interpersonal skills, attention to detail.
Benefits:
- Competitive Salary
- Flexible working hours
- Holidays (Annual leave, Casual leave, Sick leave plus bank holidays)
- Medical Insurance for Self and Immediate Family
- Gratuity
- Accidental Coverage
- Learning and development opportunities
Keywords: Job Posting, Senior Pharmacovigilance Associate, Quanticate, CRO, Clinical Trials, Data Management, Pharmaceutical, Healthcare
