Join Parexel’s Global Family: Be a Catalyst for Positive Change in Healthcare
Parexel is hiring Regulatory Affairs Consultant and Senior Regulatory Affairs Associate for Clinical Trial Regulatory Submission (CTRS) Team. am..
We’re looking for candidates with below competence:
➡4-9 years of relevant experience in Clinical Trial Regulatory Submissions.
Experience in handling clinical trial studies, playing Regulatory Lead roles for global trials and exposure to Europe region would be an added advantage.
EU CTR submission expertise will be the preferred choice.
1. R0000016241- Regulatory Affairs Consultant-
https://t.ly/9QmgS
2. R0000017931- Senior Regulatory Affairs Associate- https://t.ly/JTMer