Pharmacovigilance Coordinators – I3 RESEARCH

I3 RESEARCH

Are you considering a career in Drug Safety?

Is working for an organisation that recognises your talents and realises your potential important to you?

Imagine being part of a global organisation that touches the lives of over 70 million people worldwide.

i3 Drug Safety provides the data and services to help the pharmaceutical, medical device and related industries meet regulatory requirements and support risk management throughout the development process and beyond.

As our organisation continues to expand and succeed we are looking to increase the size of our Pharmacovigilance / Drug Safety team in Singapore with a Pharmacovigilance Coordinator with exceptional communication skills, who is both motivated and committed.

As a Pharmacovigilance Coordinator, you will be responsible for the receipt, tracking, processing and reporting of adverse event information, represent Drug Safety at project team and Investigators’ meetings, develop and maintain a working knowledge of assigned studies and ensure compliance with company policies, procedures and standards.

Pharmacovigilance Coordinators

You will require:

• Bachelor’s level degree in health sciences, pharmacy, nursing or RN, or equivalent clinical research experience.
• Experience in Pharmacovigilance, Clinical research or related field an advantage
• Ability to learn and apply Standard Operating Procedures and EU/FDA regulations pertaining to Pharmacovigilance
• Ability to establish effective relationships with sponsors, as well as team members
• Ability to successfully prioritize and work on multiple tasks

In Return we will offer you:

• A competitive remuneration package with excellent benefits including reward and recognition bonus scheme.
• A commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organization.
• The opportunity to work within a successful and friendly environment.

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