IQVIA Hiring Pharmacovigilance Consultant – Pharma/Life Sciences/Biotechnology Graduate
IQVIA, a leading healthcare market research provider, is seeking a talented Pharmacovigilance Consultant to join our Integrated Research Solutions (IRS) Team in ANZ. We are looking for candidates with a background in Pharma, Life Sciences, or Biotechnology who have 1-2 years of experience in pharmacovigilance. This role offers the opportunity to work within a highly regulated environment, driven by strict timelines and high standards of compliance.
About IQVIA
Company Overview
IQVIA is at the forefront of innovation in healthcare, providing comprehensive market research and data analytics services. Our Integrated Research Solutions (IRS) Team is renowned for its excellence in conducting qualitative and quantitative research studies, ensuring the highest standards of pharmacovigilance compliance.
Location: ANZ
Job Details
Pharmacovigilance Consultant
Position: Pharmacovigilance Consultant
Experience: Pharma/Life Sciences/Biotechnology graduate with 1-2 years in pharmacovigilance
Location: Gurugram, India
Job Responsibilities:
We are looking for a Pharmacovigilance and Data Analyst to join the Integrated Research Solutions (IRS) Team for IQVIA ANZ, one of Australia’s leading and largest healthcare market research providers. Supporting the team you will be responsible for conducting Adverse Event (AE) reporting set-up, data review for the purpose of AE submissions and project reconciliation requirements relating to pharmacovigilance compliance for both quantitative and qualitative research studies. Other activities you will be responsible for include coding of open-ended questions for quantitative studies, tabulation of study results, and generation of PowerPoint reports. A desire to work within a highly regulated environment and driven by strict timelines is essential. You will work closely with the project managers from our IRS team, client contacts, investigators, and third-party vendors throughout the entire project cycle.
Key responsibilities:
- Identify, monitor and report PV data from market research programs as per clients requirements or IQVIA’s standard operating process (SOPs).
- Ensure compliance with client requirements including training, reporting and reconciliation.
- Work closely and communicate with client’s drug safety units, other team members, fieldwork vendors, and data management team to facilitate safety reporting.
- Support IRS team to code / categorise verbatims captured via open-end questions in online surveys into key topics / themes.
- Support IRS team with any other data analysis required such as data tabulation, charting and PowerPoint generation.
Qualifications:
- Bachelor’s or Master’s degree in Pharma, Life Sciences, or Biotechnology.
- 1-2 years of experience in pharmacovigilance, preferably in primary market research.
- Strong communication skills in English, both written and verbal.
- Ability to work under pressure and meet strict deadlines.
- Proficiency in MS Word and Excel.
- Demonstrated experience in assisting project managers and working autonomously within a team.
ADDITIONAL SKILLS (highly desirable):
Experience programming / scripting online surveys using either Decipher or Confirmit/Forsta software.
How to Apply
Interested Candidates
Please apply through the referral link: IQVIA Referral Link
To apply for this job please visit referrals.iqvia.com.