As a Pharmacovigilance Services New Associate, you will be part of Accenture’s Life Sciences R&D vertical, working in the Pharmacovigilance & Drug Safety Surveillance field. This role supports biopharma companies by handling critical activities such as case processing, safety database management, and regulatory submissions.
Responsibilities:
- Case identification, data entry, MedDRA coding, and follow-up for Individual Case Safety Reports (ICSRs).
- Processing of reports in line with global regulatory requirements and client guidelines.
- Ensuring high-quality safety surveillance and drug safety reporting.
- Managing affiliate mailbox and reconciling reports as per process guidelines.
- Collaborating with your team and supervisor to ensure task completion.
- Contributing to written follow-up attempts for serious and non-serious cases.
What are We Looking for?
- Adaptability and flexibility in handling various tasks.
- Ability to perform under pressure and meet deadlines.
- Strong teamwork skills and ability to collaborate effectively.
- Commitment to delivering high-quality work with attention to detail.
- Excellent written and verbal communication skills.
Qualifications:
- BSc degree in a relevant field.
- 0 to 1 year of experience, making this an ideal role for fresh graduates.
- Proficiency in English.
Skills Required:
- Basic understanding of pharmacovigilance processes.
- Familiarity with MedDRA coding and safety databases.
- Strong data entry and processing skills.
- Ability to work in rotational shifts.
