
Regulatory Affairs Associate
3 hours ago
An exciting opportunity to work for a global CRO in a well established Regulatory team.
**Your new company**
A mid sized global CRO searching for Regulatory Affairs Professional with hands on experience with clinical trials. They are a company that focus on their employee well-being and and professional development. Their Australian head office is based in Sydney
**Your new role**
This is an exciting opportunity to join a small team of Regulatory experts. The role will focus on the facilitating the start of research products of medicinal products. You will be responsible for preparing clinical trial dossiers and ethics authorities incl import/ export license in ANZ. you will be able to communicate with Regulatory Authorities, ethics committees, relevant vendors and project teams on regulatory related matters. Review documents to IP release to sites and deliver regulatory training to project teams.
**What you'll need to succeed**
- Tertiary Qualification in science related field
- Demonstrated experience with Clinical trials
- Knowledge of TGA & Medsafe
- Experience and understanding of GCP guidelines
- Excellent communication skills.
**What you'll get in return**
You will be working in an employee centric environment, in an established and growing organisation. The roles offers an excellent salary package and benefits.
**What you need to do now**
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
**LHS 297508** #2689409
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