Global Regulatory Lead, Clinical Trials Submissions
IQVIA Argentina
IQVIA Argentina seeks a Regulatory Affairs Officer in Mexico City to serve as Regulatory Team Lead on complex global studies. The ideal candidate will draft and review regulatory documentation and engage with clients and regulatory authorities.
Applicants should have 3–4 years of clinical trial regulatory experience, a degree in Life Sciences, and proficiency with regulatory submission platforms. A problem-solving mindset and the ability to manage multiple projects in fast-paced environments are essential.
#J-18808-LjbffrVacante publicada el 3 días atrás
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